Method for total synthesis of ecteinascidins and intermediate compounds thereof

ABSTRACT

An intermediate compound for total synthesis of ecteinascidins comprising, a compound represented by general formula 2 having thioether group at C4 site, and the substituent R 2  of N 12  site is trichloroethoxicarbonyl (Troc) to which various substituents can be introduced by mild condition, further having 10 members ring structure which can be converted to a ring of other numbered members.

CROSS-REFERENCE

This application is a divisional of U.S. patent application Ser. No. 10/498,367, U.S. Pat. No. 7,417,145, filed Jun. 10, 2004, which is a §371 application of PCT/JP02/09690, filed on Sep. 20, 2002, which claims priority to JP 2002/19360, filed on Jan. 29, 2002.

FIELD OF THE INVENTION

The present invention relates to intermediate compounds useful for the total synthesis of ecteinascidin 743 (hereinafter shortened to Et 743) having high antineoplastic activity, the analogous structural compounds to Et 743 and the method for synthesis of Et 743.

BACKGROUND OF THE INVENTION

Ecteinascidins are a group of marine alkaloid having antineoplasticity which is isolated from the extracted products from the marine tunicate habitat of the Caribbean sea by a very small amount. Among the ecteinascidins, Et 743 has a very strong antineoplastic activity, studies to put it into practical use as a carcinostatic agent are limited, and the phase II clinical tests are now being carried out in ten countries in Europe and America. It is known that Et 743 has an effect of depressing the proliferation of cancer cells by 10 to 100 times more potent than (IC50=0.1-1 nM) Toxol, Camptotesin, Adriamycin or Mitomycin which are currently used carcinostatic agents.

From the background mentioned above, various studies for synthesis were carried out; however, the complete synthesis was only reported by Prof. E. J. Corey of Harvard University in the U.S.A. (J. Am. Chem. Soc. 1996, 118, 9202-9203, reference document A).

In the process of the total synthesis disclosed in Document A (refer to page 9202), the main feature of the process is that Et 743 is synthesized from the analogous compound to the compound represented by general formula 1 of the present invention via intermediates 4 and 8. That is, according to said process, the C₄ site of ring B (regarding the location of rings, and the sites of atoms comprising the 6 membered ring, refer to general formula 1), which composes a 6 membered ring, is formed from the intermediate 4 at the first step. Since the atom C₄ composing the ring B of the 6-membered ring H, which lacks reactivity, is bonded, it becomes necessary to perform an oxidation reaction at the C₄ site on the B ring. This oxidation reaction is not effective and is carried out under harsh conditions; therefore production on an industrial scale is difficult, and also the yield is not good. Further, since the atom N₁₂ site of the synthesized intermediate is substituted by an alkyl group which lacks reactivity, in this case substituted by a methyl group, it is not suited to the synthesis of various compounds. Although total synthesis was reported, the supplying source of Et 743 still depends on the natural sample whose supply is very scarce. Therefore, the establishment of the method for a large scale production of Et 743 is desired and requires accomplishing an effective synthesizing process.

Since ET 743 is known as a medicine having high antineoplasticity, and phthalascidin induced from the intermediate product at the synthesis of Et 743 displays the same activity to ET 743, the establishment of an effective and mild method for synthesis of ET 743 and analogous compounds thereof is strongly desired.

Therefore, the subject of the present invention is to accomplish the effective method for total synthesis of Et 743, and further, to provide not only Et 743 but also analogous compounds.

To dissolve the subject, the present invention uses retrosynthetic analysis for easy synthesis. It will be possible to form a B ring by a ring forming reaction at the ortho position of phenol, which binds an A ring to inner molecular aldehyde in a compound generated by the 4-8 reaction. Further, the present invention contemplates that the generated compound by the 4-8 reaction can be synthesized based on the polycondensation reaction of general formula 4, and general formula 5 via a compound of general formula 3. Then the total synthesis of Et 743, which is the aimed compound, can be accomplished by way of the compounds represented by general formulae 5, 4, 3, 2 and 1 and the specific structure of general formulae 1 and 2. This synthetic route provides for the analogous compounds of Et 743.

DISCLOSURE OF THE INVENTION

The first embodiment of the present invention is an intermediate compound for total synthesis of ecteinascidins comprising, a compound represented by general formula 1 having a thioether group at C₄ site, and the substituent R₂ of N₁₂ site is trichloroethoxicarbonyl (Troc) to which various substituents can be introduced by mild conditions, and further having a 10 membered ring structure which can be converted to a ring of other numbered members,

wherein, Y is O or NH, X₂, X₃ and X₄ are independently selected from the group consisting of H or an alkyl group of carbon number 4 or less, an alkoxyalkyl group, an allyl group, or an alkyl or arylsulfonyl group, R₁ and R₄ is H or an alkyl group of carbon number 4 or less, R₂ is an alkoxycarbonyl group which can be substituted by halogen, a lower alkyl sulfonyl group or an aryl sulfonyl group and R₃ is nitrile or OH.

The second embodiment of the present invention is a method for synthesis of the compound of general formula 1 comprising the processes displayed by the reaction 5-1, which is a transforming reaction of C₁₈ hydroxyl group to allyl ether and C₂₂ acetyl group to a hydroxyl group, the reaction 5-2, which is an introducing reaction of cysteine derivatives into C₂₂ acetyl group, and the reaction 5-3 which is a C₄ thioetherification reaction and a transforming reaction of C₅ hydroxyl group to an acetyl group, wherein Y is O, X₂ is Ac, X₃ is H, R₁ is Me, R₂ is Troc, R₃ is CN, and X₄ and R₄ are the same as in general formula 1.

The third embodiment of the present invention is an intermediate compound for total synthesis of ecteinascidins having a pentacyclic backbone of ecteinascidins, a compound represented by general formula 2 having an OH group at C₄ and the substituent R₂ of N₁₂ is trichloroethoxicarbonyl (Troc) to which various substituents can be introduced by mild conditions,

wherein, Y is oxygen or NH, X₁ is a hydroxyl group or a protecting group of an amino group, X₂, X₃ and X₄ are independently selected from the group consisting of H or an alkyl group of carbon number 4 or less, an alkoxyalkyl group, an allyl group, or an alkyl or arylsulfonyl group, R₁ and R₄ are H or an alkyl group of carbon number 4 or less, R₂ is an alkoxycarbonyl group which can be substituted by halogen, a lower alkyl sulfonyl group or an aryl sulfonyl group, and R₃ is nitrile or OH.

Desirably, the third embodiment of the present invention is the intermediate compound for total synthesis of ecteinascidins represented by general formula 2 wherein, Y is O, X₁ is selected from silyl groups consisting of an acyl group of carbon number 4 or less, TBDPS, TIPS, TBS, TES, and TMS, X₂ and X₃ are an allyloxy group, or an alkoxy group of carbon number 4 or less or an alkoxyalkoxy group, R₃ is CN and R₄ is an alkyl group of carbon number 4 or less.

The fourth embodiment of the present invention is a method for synthesis of the compound of general formula 2 consisting of the processes displayed by the reaction 4-1 which transforms C₅ mesily group to an acetyl group, the reaction 4-2 which is the transforming reaction of N₁₂ to T-butoxycarbonyl group to trichloroethyl group, the reaction of 4-3 which is a hydration reaction of C₃₋₄ double bond, the reaction 4-4 which is the transforming reaction of C₄ hydroxyl group to a TBS group and a transforming reaction of C₂₂ and C₅ acetyl group to a hydroxyl group, the reaction 4-5 which is a transforming reaction of C₅ hydroxyl group to a benzyl group, reaction 4-6 which is a reduction reaction of C₂₁ amide to a ring closing reaction of oxazolidine, the reaction 4-7 which is a ring operation reaction of oxazolidine and a transforming reaction of C₂ hydroxyl group to an aldehyde and the reaction 4-9 which is a transforming reaction of C₅, C₁₈ benzyloxy groups to a hydroxyl group and a ring forming reaction of the B ring, wherein Y is O, X₂ is H, X₃ is H, R₃ is CN, X₁ is Ac, X₄, R₁ and R₄ are the same as in the general formula 2.

The fifth embodiment of the present invention is an intermediate compound for the compound of general formula 2 represented by general formula 3 wherein the carbon at the C₁₀ site of the pentacyclic backbone of the ecteinascidins of the general formula 2 is bonded with H.

In general formula 3, R₁, R₂ and R₄, X₁-X₄ are the same as in general formula 2.

Desirably, the fifth embodiment of the present invention is the intermediate compound for the compound represented by general formula 3, wherein Y is O, X₁ is selected from the silyl groups consisting of an acyl group of carbon number 4 or less, TBDPS, TIPS, TBS, TES and TMS, X₂ and x₃ are an allyloxy group, or an alkoxy group of carbon number 4 or less, or an alkoxyalkoxy group, R₃ is CN and R₄ is an alkyl group of carbon number 4 or less.

The sixth embodiment of the present invention is the method for synthesis of the compound of general formula 3 consisting of the processes displayed by the reaction 3-1 which is Ugi's 4 component condensation reaction, the reaction 3-2 which is the transforming reaction of the C₂₂ TBTPS group to an acetyl group, the reaction 3-3 which is a C ring formation reaction, the reaction 3-4 which is a transforming reaction of C₅ hydroxyl group to a mesyl group, the reaction 3-5 which is a reduction of C₁₁ amide and a dehydration reaction of C₃₋₄ double bond and the reaction 3-6 which is the construction of D ring by a Heck reaction, wherein Y is O, X₁ is Ac, X₂ is Ms and R₂ is Boc, X₃, X₄, R₁ and R₄ are same as to the general formula 2.

The seventh embodiment of the present invention is the amine compound which provides a segment forming a chemical structure site of the A ring side of the intermediate compound of general formula 3 represented by general formula 4 by Ugi reaction.

In general formula 4, R₄, X₂, Y and X₁ are the same as in general formula 2.

Desirably, the seventh embodiment of the present invention is the amine compound, wherein Y is O, X₁ is selected from the group of silyl groups consisting of an acyl group of carbon number 4 or less, TBDPS, TIPS, TBS, TES and TMS.

The eighth embodiment of the present invention is a method for synthesis of the compound of general formula consisting of the processes displayed by the reaction 2-1 which is the transforming reaction from C₅ hydroxyl group to a methoxymethyl group, reaction 2-2 which is the introducing reaction of a hydroxyl group to C₂₂, reaction 2-3 which is the Mannich reaction, reaction 2-4 which is the transforming reaction of C₆ hydroxyl group to a trifluoromethanesulfonyl group (Tf), reaction 2-5 which is the reducing reaction of lactone, reaction 2-6 which is the transforming reaction of C₂₂ hydroxyl to a TBDPS group, reaction 2-7 which is the methylatino reaction of C₆ to a TfO group and the reaction 2-8 which is the transforming reaction to amine, wherein Y═O, X₁ is TBDPS, X₂ is MOM and R₄ is Me.

The ninth embodiment of the present invention is the carboxylic acid compound which provides a segment forming a chemical structural site on the ring side of the intermediate compound of general formula 3 represented by general formula 5 by Ugi reaction.

In general formula 5, R₁, R₂, X₃ and X₄ are the same as in general formula 1.

Desirably, the ninth embodiment of the present invention is the carboxylic acid compound wherein, X₃ and X₄ are independently selected from the group consisting of H or an alkyl group of carbon number 4 or less, an alkoxyalkyl group, an allyl group, an alkyl or arylsulfonyl group, R₂ is an alkoxycarbonyl group, a lower alkylsulfonyl or an arylsulfonyl group which can be substituted by halogen.

The tenth embodiment of the present invention is the method for synthesis of the compound of general formula 5 consisting of the processes displayed by the reaction 1-1 which is the introducing reaction of a formyl group to C₂₀, the reaction 1-2 which is the transforming reaction of the C₂₀ formyl group to dimethylacetal, the reaction 1-3 which is the iodination reaction of C₁₉ and an acidic hydrolysis reaction, the reaction 1-4 which is the transforming reaction of C₁₈ hydroxyl group to a benzyl group, the reaction 1-5 which is an Honor-Emons reaction, reaction 1-6 which is the asymmetric reducing reaction by a Duphos-Rh synthetic catalyst and reaction 1-7 which is the hydrolysis reaction of methylester, wherein R₂ is Boc, X₃ is Bn, X₄ is Me, the ring and R₁ is the same in general formula 2.

DESCRIPTION OF THE PREFERRED EMBODIMENT

The present invention will be illustrated more in detail according to the following description.

-   A. As mentioned above, the first feature of the present invention is     the B ring forming reaction at the ortho position of phenol which     binds A ring to aldehyde by reaction 4-9 in the synthesis process of     the compound of the general formula 2. The feature of this reaction     is that the reaction is progressed by a mild, neutralized condition.     Having an OH group at the C₄ site which is expressed as the     structural feature of the compound represented by general formula 2,     the mild reaction condition is superior. Since the compound     disclosed in the above-mentioned prior art has hydrogen at this     site, a reaction under harsh conditions is required. Furthermore,     from this intermediate synthesis, the synthesis of various analogous     compounds is possible, and it is possible to obtain a compound     having antineoplastic activity, such as au phtharasacidin being     equal to Et 743. -   B. The second feature of the present invention requires using the     Ugi's 4 component reaction and the Heck reaction of reaction 3-6 as     the key process. First, in the Ugi's 4 component condensation     reaction of reaction 3-1, no condensation reagents are required for     the generation of an amide bone. The compound of reaction 3-1 makes     it possible to progress easily to the formation of the C ring of     reaction 3-3. The ring forming reaction of reaction 3-6 not only     controls the stereochemistry of C₃ site perfectly, but also can be     performed using a catalytic amount of Pd₂(dba)₃, which is an     expensive reagent, by catalytic amount. -   C. The third feature of the present invention is that the amine     represented by general formula 4 and the carboxylic acid represented     by general formula 5 can be made by large scale production. -   D. The fourth feature of the present invention is the ring forming     reaction of a 10 membered ring shown by the reaction 5-3 process     that is caused by bonding of a sulfur atom at the C₄ site. In the     compound of the present invention, a hydroxyl group is introduced to     the C₄ site, and it is possible to generate a cation of the benzyl     site easily under the acidic condition. Therefore, the ring     formation of a 10 membered ring by bonding the sulfur atom to said     cation is produced with high yield. When compared with the case     which uses the compound whose C₄ site is H, reported by Prof. E. J.     Corey, the method of the present invention can use a more mild     condition. Therefore, the method of the present invention has the     advantage of easily accomplishing larger scale production, and     further has the capability of introducing the ring of various     numbers of members and is useful for the synthesis of various     derivatives.

EXAMPLE

The present invention will be illustrated more in detail according to the specified Examples. However, these Examples are intended to provide easily understanding of the present invention and are not intending to limit the scope of the claim of the present invention.

Example 1

The synthesis of compound 2-8, wherein Y contained in general formula 4 is O, X₁ contained in general formula 4 is TBDPS, X₂ contained in general formula 4 is MOM and R₄ contained in general formula 4 is Me. The reaction process and the whole chemical formula of the generated compounds in each reaction process are shown by the following synthesis process A.

Detail of Synthetic Process A; (1) Synthesis of Compound 2-1

NaH (40 g, 1.0 mol) was dispersed in 700 ml of the mixed solution of THF and DMF (5:2), THF solution (300 ml) of 3,4-methylenedioxyphenol (138 g, 1.0 mol) was dropped at 0° C. After stirred at room temperature for 30 minutes, MOMCl (84.5 g, 1.05 mol) was dropped and stirred at room temperature for 1 hour. Hexane and water were added to the reaction solution and the organic layer was separated. After the water layer was extracted by hexane, the organic layer was concentrated by vacuum. The residue was dissolved in hexane, washed by brine, then dried by Na₂SO₄. After concentrated by vacuum, the residue was distilled by vacuum (103° C./0.35 mmHg), and the compound 2-1 (177 g, 0.97 mol, 97%) was obtained as a colorless oil. The physical property of compound 2-1 is shown in Table 1.

TABLE 1 Compound 2-1 IR (neat film) 1244, 1215, 1176, 1153, 1099, 1069, 1040, 1004, 940, 922, 842, 813 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 6.71 (d, J = 8.4 Hz, 1H) 6.63 (s, 1H), 6.49 (d, J = 8.4 Hz, 1H), 5.90 (s, 2H), 5.08 (s, 2H), 3.46 (s, 3H); ¹³C NMR (100 MHz, CDCl₃), δ 152.5, 148.1, 142.5, 108.4, 108.0, 101.2, 99.7, 95.4, 55.8. Synthesis of Compound 2-2

After n-BuLi (3.02 mol n-hexane solution, 11.0 ml, 33.2 mmol) was dropped in THF (100 ml) solution of compound 2-1 (5.44 g, 29.9 mmol) at 0° C., the temperature was elevated to room temperature. The reaction solution was cooled down to 0° C., B(OOMe)₃ (4.10 ml, 36.1 mmol) was added, then AcOH(3.4 ml, 59 mmol) and aqueous solution of 7% H₂O₂ (26 ml, 60 mmol) were added. The reaction solution was stirred for 4.5 hours at room temperature, saturated aqueous solution of (NH₄)₂SO₄ (100 ml) and saturated aqueous solution of Na₂SO₃ (100 ml) were added, and an organic layer was dried with MgSO₄ then concentrated by vacuum. The residue was purified by silica gel chromatography (70% EtOAc in n-haxane), and the compound 2-2 (5.42 g 27.3 mmol) was obtained as a colorless oil. The physical property of compound 2-2 is shown in Table 2.

TABLE 2 Compound 2-2 IR (neat film) 3439, 1652, 1493, 1292, 1245, 1157, 1044, 932, 791 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 6.55 (d, J = 8.4 Hz, 1H), 6.45 (br, 1H), 6.32 (d, J = 8.4 Hz, 1H), 5.94 (s, 2H), 5.09 (s, 2H), 3.50 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 144.3, 141.3, 134.4, 132.0, 109.2, 101.6, 99.1, 97.3, 60.4, 56.3 Synthesis of Compound 2-3

As the method for synthesis of agent lactone (agent-1) which is added in the reaction 2-3, document, for example, [“Synthesis of Optically Active Arylglycines; Stereoselective Mannich Reaction of Phenols with a New Chiral template,” S. Tohma, A. Endo, T. Kan, T. Fukuyama, Synlett, 1479-1499 (2001).] can be mentioned.

In CH₂Cl₂ (200 ml) solution of the compound 2-2 (19.8 g, 100 mmol) and agent-1 (20.3 g, 100 mmol), TFA (38 ml, 0.49 mol, 5 equiv) was dropped by 1.5 hours at −10° C. After the reaction solution was stirred for 40 minutes at room temperature, Na₂CO₃ (40 g, 0.38 mol, 3.8 equivalent) and H₂O (200 ml) were added and extracted by CH₂Cl₂. The water layer was extracted by CH₂Cl₂, then the organic layer was washed by brine, dried by Na₂SO₄ and concentrated by CH₂Cl₂. The residue was purified by silica gel chromatography (30% EtOAc in n-haxane), and the compound 2-3 (35.6 g 89 mmol, 89%) was obtained a colorless oil. The physical property of compound 2-3 is shown in Table 3.

TABLE 3 Compound 2-3 [α]_(D) ²⁷ −75.2° (c = 1.65, CHCl₃); IR (neat film) 3327, 1724, 1506, 1457, 1299, 1151, 1118, 1082, 1049, 1101, 934 cm⁻¹;¹H NMR (400 MHz, CDCl₃) δ 7.29-7.37 (m, 5H), 6.51 (s, 1H) 5.93 (s, 1h), 5.91 (d, J = 8.0 Hz, 1H), 5.05 (d, J = 8.0 Hz, 1H), 5.03 (s, 1H) 4.15 (s, 1H), 3.51 (s, 3H), 2.03 (br, 1H), 1.37 (s, 6H); ¹³C NMR (100 MHz, CDCl₃) δ 169.0, 141.8, 141.4, 138.2, 134.8, 132.4, 128.4, 128.3, 128.3, 111.6, 110.0, 101.9, 86.7, 61.0, 57.1, 56.4, 26.6, 22.0; Synthesis of Compound 2-4

To the solution of the compound 2-3 (242 mg, 0.603 mmol) and pyridine (0.15 ml, 1.9 mmol), Tf₂O (0.13 ml, 0.77 mmol, 1.3 equivalent) was dropped at 0° C. After the reacted product was stirred for 5 minutes, the aqueous solution of saturated NaHCO₃ was added and extracted by EtOAc. The organic layer was washed by the aqueous solution of 1N HCl and the saturated aqueous solution of NaHCO₃, then dried by MgSO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane), and the compound 2-4 (290 mg, 0.544 mmol, 90%) was obtained as a colorless oil. The physical properties of the compound 2-4 are shown in Table 4.

TABLE 4 Compound 2-4 [α]_(D) ²⁶ −32.1° (c = 2.59, CHCl₃); IR (neat film) 3333, 1733, 1496, 1462, 1427, 1299, 1216, 1138, 1056, 999, 979, 936, 832 cm⁻¹;¹H NMR (400 MHz, CDCl₃) δ 7.32-7.40 (m, 5H), 6.71 (s, 1H) 6.06 (s, 1H), 6.03 (s, 1H), 5.19 (d, J = 5.8 Hz, 1H), 5.14 (d, J = 5.8 Hz, 1H), 5.09 (s, 1H) 4.23 (s, 1H), 3.49 (s, 3H), 2.01 (br, 1H), 1.40 (s, 6H); ¹³C NMR (100 MHz, CDCl₃) δ 167.8, 144.9, 141.2, 140.2, 137.8, 128.3, 128.2, 128.1, 123.1, 120.2, 116.7, 108.0, 103.1, 95.9, 86.7, 61.3, 56.9, 56.3, 26.4, 21.8 Synthesis of Compound 2-5

To the MeOH (50 ml) solution of the compound 2-4 (4.70 g, 8.8 mmol), NaBH₄ was added at 0° C. and stirred for 30 minutes. To the reaction solution, EtOAc (300 ml) was added and washed by 1N HCl (100 ml). The organic layer was washed by saturated aqueous solution of NaHCO₃, and after dried by MgSO₄, concentrated by vacuum. The residue was purified by silica gel chromatography (in 60% EtOAc n-hexane), and the compound 2-5 (4.04 g, 7.5 mmol, 85%) was obtained as a colorless oil. The physical properties of the compound 2-5 are shown in Table 5.

TABLE 5 Compound 2-5 [α]_(D) ²⁷ −102°(c = 1.67, CHCl₃); IR (neat film) 3398, 1497, 1456, 1426, 1218, 1136, 1054, 937, 833 cm⁻¹; 1H NMR (400 MHz, CDCl₃) δ 7.25-7.33 (m, 5H), 6.63 (s, 1H) 5.94 (s, 1H), 5.93 (s, 1H), 5.11 (d, J = 6.8 Hz, 1H), 5.07 (d, J = 6.8 Hz, 1H), 3.65 (br, 1H), 3.52-3.64 (br, 2H), 3.50 (s, 3H), 3.39 (s, 1H), 2.71 (br, 1H), 1.11(s, 6H); ¹³C NMR (100 MHz, CDCl₃) δ 144.8, 141.6, 139.9, 139.2, 128.7, 128.1, 127.5, 122.4, 120.9, 120.1, 116.9, 107.1, 102.9, 95.6, 72.7, 68.9, 64.9, 56.9, 56.3, 27.9, 23.8; Synthesis of Compound 2-6

To DMF solution of the compound 2-5 (1.00 g, 1.86 mmol) and imidazole (0.63 g, 9.3 mmol), TBDPSCl (1.22 ml, 4.7 mmol) was added and stirred at room temperature. To the reacted product, Et₂O and water were added and the organic layer was washed by brine, dried by Na₂SO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 10% EtOAc n-hexane), and the compound 2-6 (1.31 g, 1.69 mmol, 91%) was obtained as a colorless oil. The physical properties of the compound 2-6 are shown in Table 6.

TABLE 6 Compound 2-6 [α]_(D) ²⁷ −75.2°(c = 1.65, CHCl₃); IR (neat film) 3445, 1469, 1428, 1363, 1263, 1109, 1062, 991, 944, 826 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.61 (d, J = 8.0 Hz, 2H), 7.56 (d, J = 8.0 Hz, 2H), 7.23-7.42 (m, 11H), 6.62 (s, 1H), 5.83 (s, 2H), 5.10 (d, J = 6.8 Hz, 1H), 5.08 (d, J = 6.8 Hz, 1H), 3.77 (dd, J = 6.0, 6.8 Hz, 1H), 3.67 (m, 2H), 3.47 (s, 3H), 3.37 (s, 1H), 3.34 (br, 1H), 1.909 (s, 6H), 1.08 (s, 9H); ¹³C NMR (100 MHz, CDCl₃) δ 144.7, 141.8, 139.8, 139.5, 135.6, 132.9, 129.7, 128.5, 128.1, 127.7, 127.6, 127.4, 122.5, 121.0, 120.1, 116.9, 107.7, 102.7, 95.8, 72.2, 68.6, 66.4, 56.8, 56.3, 27.4, 26.8, 24.2, 19.2; Synthesis of Compound 2-7

To the THF (105 ml) solution of the compound 2-6 (16.7 g, 21.5 mmol), MeZnCl (2.0M in THF solution, 37.5 ml, 75.1 mmol) was added at 0° C. After the temperature of the reaction solution was elevated to room temperature, PdCl₂ (dppf) (314 mg, 0.43 mmol) was added and refluxed by heating for 13.5 hours. EtOAc was added to the reaction solution, then washed by 1N HCl aqueous solution, saturated aqueous solution of NaHCO₃ and brine. The organic layer was dried by Na₂SO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 10% EtOAc n-hexane), and the compound 2-7 (13.4 g, 20.9 mmol, 97%) was obtained as a white solid. The physical properties of the compound 2-7 are shown in Table 7.

TABLE 7 Compound 2-7 [α]_(D) ²⁶ −99.3° (c = 0.81, CHCl₃); IR (neat film) 3457, 2931, 1494, 1457, 1427, 1362, 1216, 1139, 1110, 1056, 1006, 936, 828 cm⁻¹;¹H NMR (400 MHz, CDCl₃ δ 7.63 (d, J = 6.8 Hz, 2H), 7.56, (d, J = 6.8 Hz, 2H), 7.22-7.47 (m, 11H), 6.30 (s, 1H), 5.77 (s, 2H), 5.03 (d, J = 5.6Hz, 1H), 5.01 (d, J = 5.6 Hz, 1H), 3.83 (dd, J = 10.8, 10.8, 1H), 3.61-3.66 (m, 2H), 3.44 (s, 3H), 3.38 (s, 1H), 2.08 (s, 3H), 1.09 (s, 9H), 1.06 (s, 6H); ¹³C NMR (100 MHz, CDCl₃) δ 150.8, 146.6, 140.0, 139.7, 135.6, 135.6, 133.2, 133.1, 130.9, 130.4, 130.0, 129.7, 129.6, 128.5, 128.4, 128.0, 127.7, 127.6, 127.2, 117.7, 109.6, 107.0, 100.8, 95.6, 72.1, 68.5, 66.6, 57.7, 56.0, 27.3, 26.8, 24.0, 19.2, 8.8 Synthesis of Compound 2-8

To the CH₃CN (12 ml) solution of the compound 2-7 (640 mg, 1.0 mmol), Pb(OAc)₄ (0.56 g, 1.26 mmol) was added slowly at 0° C. To the reaction solution, saturated aqueous solution of NaHCO₃ was added and extracted by EtOAc. The organic layer was washed by brine, dried by Na₂SO₄, concentrated by vacuum and crude product was obtained. The obtained crude product was dissolved in EtOH (10 ml), then hydrochloric acid salt of hydroxylamine (347 mg, 5.6 mmol) and sodium acetate (410 mg, 5.0 mmol) were added at room temperature and stirred for 1.5 hours. EtOAc was added to the reaction solution, then filtrated by celite and concentrated by vacuum. The residue was dissolved with EtOAc and washed by 1N HCl aqueous solution, saturated aqueous solution of NaHCO₃ and brine. After the organic layer was dried by Na₂SO₄, concentrated by vacuum. The residue was purified by silica gel chromatography (EtOAc), and the compound 2-8 (436 mg, 0.88 mmol, 89%) was obtained. The physical properties of the compound 2-8 are shown in Table 8.

TABLE 8 Compound 2-8 [α]_(D) ²³−1.99° (c = 1.30, CHCl₃); IR (neat film) 1440, 1115, 1062, 991, 938, 826 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.61-7.65 (m, 4H), 7.35-7.45 (m, 6H), 6.57 (s, 1H), 5.81 (s, 2H), 5.09 (s, 2H), 4.16 (dd, J = 6.8, 4.8 Hz, 1H), 3.87 (dd, J = 10.0, 4.8 Hz, 1H), 3.76 (dd, J = 10.0, 6.8 Hz, 1H), 3.48 (s, 3H), 2.14 (s, 3H), 1.08 (s, 9H); ¹³C NMR (100 MHz, CDCl₃) δ 150.8, 146.1, 139.1, 135.5, 135.5, 133.4, 133.3, 129.5, 129.5, 127.5, 120.7, 109.1, 105.8, 100.7, 95.7, 68.1, 55.9, 53.4, 26.7, 19.1, 8.8

Example 2

Synthesis of the Compound 1-7 Contained in General Formula 5

The process for synthetic reaction and the chemical structure of the products obtained at each process are totally shown in following synthesis process B.

Detail of Synthesis of the Compound 1-7

Regarding the synthesis of bromide (starting material-1), for example, document of [“Synthetic Study on Ectenascidin 743 starting from D-glucose” A. Entoh, T. Kan, and T. Fukuyama, Synlett, 1103-1105 (1999)] can be mentioned.

Synthesis of Compound 1-1

To the THF solution (900 ml) of the starting material-1 (114 g, 437 mmol), n-BuLi (2.46M in n-hexane solution, 270 ml, 664 mmol) was added at −78° C., then DMF (170 ml, 2.20 mol) was added. The temperature of the reaction solution was elevated to room temperature, and water was added to the reaction solution, then concentrated by vacuum. Et₂O was added to the residue, and washed by saturated aqueous solution of NaHCO₃ and brine. After dried by MgSO₄, concentrated by vacuum. The residue was purified by silica gel chromatography (30% Et₂O in n-hexane), and the compound 1-1 (73.0 g, 347 mmol, 79%) was obtained as a colorless oil. The physical properties of the compound 1-1 are shown in Table 9.

TABLE 9 Compound 1-1 IR (neat film) 1699, 1585, 1488, 1451, 1382, 1299, 1235, 1155, 1133, 1099, 1051, 1003, 928, 863 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 9.83 (s, 1H), 7.49 (s, 1H), 7.36 (s, 1H), 5.25 (s, 2H), 3.90 (s, 3H), 3.51 (s, 3H), 2.31 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 191.2, 153.5, 150.5, 132.8, 132.1, 126.9, 114.2, 95.0, 60.3, 56.3, 16.0 Synthesis of Compound 1-2

To the MeOH solution (5.0 ml) of the compound 1-1 (331 mg, 1.57 mmol) and CH(OMe)₃ (1.0 ml, 9.14 mol), CSA (20.2 mg, 0.09 mmol) was added and refluxed by heating for 1 hour. K₂CO₃ (103 mg, 0.75 mmol) was added to the reaction solution and concentrated by vacuum. The residue was dissolved in Et₂O and filtrated by a column of basic alumina. After concentrated by vacuum, the compound 1-2 (381 mg, 1.49 mmol, 94%) was obtained as a colorless oil. The obtained compound 1-2 was used to the next reaction without refining. The physical properties of the compound 1-2 are shown in Table 10.

TABLE 10 Compound 1-2 1H NMR (400 MHz, CDCl₃) δ 7.05 (s, 1H), 6.93 (s, 1H), 5.27 (s, 1H), 5.25 (s, 2H), 3.89 (s, 3H), 3.59 (s, 3H), 3.34 (s, 3H), 2.32 (s, 3H) Synthesis of Compound 1-3

To the Et₂O solution (4.0 ml) of the compound 1-2 (381 mg, 1.49 mmol), n-BuLi (2.46M in n-hexane solution, 0.95 ml, 2.34 mmol) was added at 0° C., then the temperature was elevated to room temperature. After reduced the temperature of the reaction solution to 0° C., Et₂O (3.0 ml) solution of I₂ (648 mg, 2.55 ml) was added. After water and saturated aqueous solution of NaHCO₃ were added, extracted by EtOAc. The organic layer was washed by brine, dried by MgSO₄ and concentrated by vacuum. The residue was dissolved by THF (5.0 ml) and 12N HCl (2.0 ml) aqueous solution was added at room temperature. After stirred for 15 minutes, neutralized by saturated aqueous solution of NaHCO₃ and extracted by EtOAc. The organic layer was washed by saturated aqueous solution of brine, dried by MgSO₄ and concentrated. The residue was dissolved by CH₂Cl₂ and filtrated by silica gel and concentrated by vacuum. The obtained solid was washed by n-hexane and the compound 1-3 (314 mg, 1.07 mmol, 72%), and the compound 1-3 was obtained as a colorless solid. The physical properties of the compound 1-3 are shown in Table 11.

TABLE 11 Compound 1-3 IR (neat film) 3389, 1670, 1583, 1464, 1412, 1299, 1247, 1127, 997 cm⁻¹; ¹H NMR 400 MHz, CDCl₃) δ 10.0 (s, 1H), 7.37 (s, 1H), 6.43 (bs, 1H), 3.89 (s, 3H), 2.32 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 194.9, 149.9, 149.2, 131.3, 130.9, 125.3, 125.3, 60.8, 15.8; The Synthesis of Compound 1-4

To the CH₃CN (3.0 ml) solution of the compound 1-3 (325 mg, 1.11 mmol) and K₂CO₃ (465 mg, 3.37 mmol) BuBr (140 μl, 1.18 mmol) were added at room temperature and refluxed by heating for 40%. After CH₂Cl₂ were added to the reaction solution, filtrated by Celite, then concentrated by vacuum. The residue was purified by silica gel chromatography (50% CH₂Cl₂ in n-hexane), and the compound 1-4 (415 mg, 1.09 mmol, 98%) was obtained as a colorless oil. The physical properties of the compound 1-4 are shown in Table 12.

TABLE 12 Compound 1-4 IR (neat film) 1684, 1576, 1464, 1303, 1153, 1068, 1005 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 10.0 (s, 1H), 7.60 (d, 8.0 Hz, 2H), 7.59 (s, 1H), 7.30-7.45 (m, 3H), 5.01 (s, 2H), 3.93 (s, 3H), 2.30 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 195.3, 157.1, 151.3, 136.3, 133.3, 131.3, 128.7, 128.5, 128.4, 128.2, 98.2, 74.9, 60.6, 15.7; The Synthesis of Compound 1-5

To the CH₂Cl₂ solution (100 ml) of the compound 1-4 (8.30 g, 21.7 mmol) and methyl-2-butoxycarbonylamino-dimethylsulfonoacetate (7.76 g, 26.1 mmol), TMG (4.10 ml, 32.7 mmol) was added at room temperature and stirred for 24 hours at room temperature. The reaction solution was washed by 10% citric acid and saturated aqueous solution of NaHCO₃, then the organic layer was dried by MgSO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography, and the compound 1-5 (11.2 g, 20.2 mmol, 1.93%) was obtained as a yellow crystal. The further refining was carried out by re-crystallization (EtOAc/n-hexane). The physical properties of the compound 1-5 are shown in Table 13.

TABLE 13 Compound 1-5 IR (neat film) 3336, 1717, 11457, 1367, 1249, 1160, 1065, 1003 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.60 (d, J = 6.8 Hz, 2H), 7.36-7.60 (m, 3H), 7.24 (s, 1H), 7.20 (s, 1H), 5.00 (s, 2H), 3.88 (s, 3H), 3.86 (s, 3H), 2.23 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 165.6, 152.4, 151.6, 136.8, 134.2, 132.5, 131.7, 128.7, 128.4, 128.2, 126.8, 125.4, 96.9, 80.9, 74.6, 60.5, 52.7, 28.0, 15.8 The Synthesis of Compound 1-6

The EtOAC solution (30 ml) of frozen and degased compound 1-5 (5.04 g, 9.10 mmol) and Rh [(COD)-(S,S)-Et-DuPHOS)] ⁺TfO⁻ (99.0 mg, 0.14 mmol, 1.5 mol %) was poured into a high pressure reactor and stirred for 22 hours under hydrogen atmosphere of 500 atm at 50° C. The reaction solution was concentrated by vacuum and the residue was purified by silica gel chromatography (50% EtOAc in n-hexane), and the compound 1-6 (5.01 g, 902 mmol, 99%) was obtained as a light yellow crystal.

Wherein, (S,S)-Et-DuPhos-catalyst Rh{[(COD)-(S,S)-Et-DuPHOS]⁺TfO⁻} is shown as follows.

The physical properties of the compound 1-6 are shown in Table 14.

TABLE 14 Compound 1-6 [α]_(D) ²⁷+7.4° (c = 1.09, CHCl₃); R (neat film) 3374, 1764, 1711, 1510, 12457, 1363, 1162, 1068, 1003 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.60 (d, J = 8.8 Hz, 2H), 7.32-7.45 (m, 3H), 6.85 (s, 1H), 5.06 (d, J = 8.8 Hz, 1H), 4.99 (s, 1H), 4.62 (ddd, J = 9.2, 8.8, 5.6 Hz, 1H), 3.82 (s, 3H), 3.72 (s, 3H), 3.28 (dd, J = 14.4, 5.6 Hz, 1H), 3.09 (dd, J = 14.4, 9.2 Hz, 1H), 2.23 (s, 3H), 1.43 (s, 9H); ¹³C NMR (100 MHz, CDCl₃) δ 172.4, 154.9, 151.7, 150.4, 136.9, 135.4, 132.3, 128.6, 128.4, 128.1, 127.8, 97.0, 79.8, 74.5, 60.4, 53.8, 52.3, 42.7, 28.2, 15.6; The Synthesis of Compound 1-7

LiOH (750 mg, 17.9 mmol, 2.0 equivalent) was added to the mixed solution of compound 1-6 (5.01 g, 9.02 mmol) in MeOH (40 ml), H₂O (10 ml) and THF (10 ml) at 0° C. Benzene was added to the reaction solution and concentrated by vacuum. 10% of aqueous solution of citric acid was added to the residue and extracted by EtOAc. Organic layer was washed by brine and dried by MgSO₄ and concentrated by vacuum. Thus the compound 1-7 (4.90 g, 9.05 mmol, 100%) was obtained as a white solid. The physical property of the compound 1-7 is shown in Table 15.

TABLE 15 Compound 1-7 [α]_(D) ²⁷−14.1° (c = 5.00, CHCl₃); IR (neat film) 3309, 2560, 1716, 1497, 1471, 1404, 1368, 1307, 1243, 1163, 1063, 1008, 907, 845, 804 cm⁻¹; 1H NMR (400 MHz, CDCl₃) δ 7.61 (br, 2H), 7.36-7.44 (br, 3H), 6.90 (s, 1H), 5.00 (br, 2H), 4.63 (br, 1H), 3.83 (s, 3H), 3.43 (br, 1H), 2.94-3.20 (br, 1H), 2.25 (s, 3H), 1.10-1.40 (br, 9H); ¹³C NMR (100 MHz, CDCl₃) δ 176.2, 175.4, 156.7, 155.2, 151.4, 150.4, 150.3, 136.9, 135.8, 135.3, 132.3, 132.2, 128.7, 128.6, 128.4, 128.4, 128.1, 127.9, 97.1, 96.7, 81.1, 80.1, 77.2, 74.5, 60.4, 60.3, 54.1, 53.8, 53.7, 44.6, 42.3, 42.2, 42.2, 28.2, 27.9, 15.6.

Example 3

The processes for synthesis of the compound 3-6 contained in general formula 3 and whole products in each process are shown in following synthetic process C.

Detail of Synthesis of C; Synthesis of Compound 3-1

To the MeOH solution (200 ml) of compound 2-8 (9.63 g, 19.5 mmol), compound 1-7 (10.57 g, 19.5 mmol) and p-methoxyphenylisocyanide (3.90 g, 29.3 mmol, 1.5 equivalent), acetoaldehyde (22 ml, 0.39 mol, 20 equivalent) was added at room temperature and refluxed for 1 hour. After concentrated by vacuum, residue was purified by silica gel chromatography (40% EtOAc, n-hexane) and compound 3-1 (21.02 g, 17.6 mmol, 90%) was obtained as a yellow solid. The physical properties of 3-1 are shown in Table 16.

TABLE 16 Compound 3-1 IR (neat film) 3315, 1699, 1687, 1511, 1463, 1428, 1367, 1245, 1159, 1112, 1062, 826 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 8.60-9.20 (m, 1H), 7.25-7.75 (m, 17H), 6.50-7.20 (m, 4H), 4.80-5.85 (m, 9H), 3.90-4.80 (m, 3H), 3.60-3.85 (m, 6H), 3.40-3.50 (m, 3H), 2.90-3.50 (m, 2H), 1.85-2.25 (m, 6H), 0.75-1.50 (m, 21H); ¹³C NMR (100 MHz, CDCl₃) δ 173.4, 172.0, 171.3, 170.1, 168.7, 167.9, 156.2, 156.1, 155.9, 155.6, 155.3, 154.3, 151.5, 151.4, 151.3, 151.0, 150.9, 150.8, 150.5, 150.1, 150.0, 146.9, 146.5, 139.8, 139.7, 136.8, 136.7, 136.6, 136.5, 135.6, 135.5, 135.4, 135.3, 135.2, 132.6, 132.5, 132.4, 132.2, 132.1, 132.0, 131.6, 131.1, 131.0, 129.9, 129.7, 129.6, 129.3, 128.5, 128.4, 128.3, 128.2, 128.0, 127.9, 127.7, 127.5, 127.4, 127.3, 123.0, 121.7, 121.5, 120.5, 113.7, 113.5, 113.4, 113.3, 113.1, 110.9, 106.2, 106.0, 100.9, 100.6, 97.5, 96.7, 96.6, 96.2, 95.8, 95.5, 95.3, 80.6, 80.5, 80.3, 79.3, 79.0, 74.4, 74.3, 71.5, 70.4, 62.6, 62.5, 60.2, 60.1, 59.7, 57.2, 56.2, 56.1, 55.9, 55.1, 54.5, 54.4, 51.5, 51.3, 42.9, 41.8, 41.1, 41.1, 28.1, 28.0, 27.9, 27.8, 27.1, 27.0, 26.9, 26.4, 19.1, 19.0, 18.9, 17.8, 17.1, 15.4, 15.3, 15.2, 15.1, 14.9, 14.8, 8.8 8.7, 8.5; Synthesis of Compound 3-2

TBAF (1M THF solution, 20 ml, 20.0 mmol) was added to THF solution (200 ml) of compound 3-1 (21.02 g, 17.6 mmol) was added at room temperature and stirred for 30 minutes. The mixed solvent of EtOH and n-hexane (3:7) was added and concentrated by vacuum. The residue was purified by silica gel chromatography (EtOAc) and yellow solid (14.90 g, 15.6 mmol, 89%) was obtained. DMPA (97 mg, 0.79 mmol) was added to the mixed solution of acetic anhydride (30 ml) of alcohol (14.90 g, 15.6 mmol) and pyridine (60 ml) and stirred for 30 minutes at 50° C. After concentrated by vacuum, residue was purified by silica gel chromatography (60%, EtOAc n-hexane) and the compound 3-2 (14.54 g, 14.6 mmol, 93%) was obtained as yellow solid. The physical properties of compound 3-2 are shown in Table 17.

TABLE 17 Compound 3-2 IR (neat film) 3318, 1743, 1700, 1511, 1436, 1368, 1304, 1245, 1170, 1112, 1060, 830 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 8.90-9.30 (m, 1H), 7.55 (d, J = 6.8 Hz, 2H), 7.20-7.50 (m, 5H), 6.30-7.20 (m, 2H), 6.80 (d, J = 6.8 Hz, 2H), 5.84-5.88 (br, 2H), 5.60-5.80 (m, 2H), 5.20-5.45 (m, 2H), 5.00-5.20 (m, 2H), 4.93-4.97 (m, 2H), 4.70-4.90 (m, 1H), 4.40-4.70 (m, 1H), 3.65-3.80 (m, 6H), 3.35-3.50 (m, 3H), 2.90-3.35 M, 1H), 1.80-2.25 (m, 9H), 1.10-1.55 (m, 12H); ¹³C NMR (100 MHz, CDCl₃) δ 173.6, 173.2, 172.7, 172.0, 170.1, 170.0, 169.7, 169.5, 169.5, 169.4, 168.2, 156.4, 156.1, 155.8, 155.2, 154.3, 151.5, 151.3, 151.2, 151.2, 151.1, 150.6, 150.3, 147.1, 146.8, 146.6, 140.0, 139.8, 139.3, 136.8, 136.7, 136.7, 136.5, 135.0, 134.9, 134.6, 132.5, 132.0, 131.1, 131.0, 128.8, 128.5, 128.4, 128.4, 128.3, 128.2, 128.1, 128.0, 127.9, 121.8, 121.8, 121.8, 121.6, 121.4, 121.2, 120.6, 113.9, 113.9, 113.8, 113.5, 113.1, 112.6, 112.1, 111.7, 111.3, 105.9, 105.7, 105.3, 101.1, 101.0, 100.7, 96.8, 96.5, 95.4, 95.1, 79.6, 79.1, 74.4, 70.6, 62.0, 60.3, 60.2, 57.3, 56.5, 56.2, 56.0, 55.8, 55.2, 50.6, 50.1, 43.5, 28.1, 28.0, 27.9, 27.8, 20.9, 20.7, 17.6, 15.3, 14.8, 8.8; Synthesis of Compound 3-3

To the CH₂Cl₂ (290 ml) solution of compound 3.2 (14.5 g, 14.5 mmol) and anisole (79 ml, 0.73 mol), TFA (58 ml, 0.75 mol) was added at 0° C., then stirred at room temperature for 9 hours. 7% Na₂SO₄ aqueous solution was added to the reaction solution and extracted by EtOAc. The organic layer was washed by saturated aqueous solution of NaHCO₃ and by brine, dried by MgSO₄ and concentrated to 300 ml, then heat refluxed for 1 hour. The solvent was evaporated off by vacuum, and the residue was purified by column chromatography (in 70% EtOAc m-hexane). Thus the compound 3-3 (19.7 g, 27.0 mmol, 87%) was obtained as a brownish powder. The physical property of the compound 3-3 is shown in Table 18.

TABLE 18 Compound 3-3 minor isomer; IR (neat film) 3345, 1752, 1683, 1652, 1456, 1306, 1232, 1093, 1037, 1007 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.56 (d, J = 8.2, 2H), 7.38-7.41 (m, 3H), 6.85 (s, 1H), 6.23 (s, 1H), 6.20 (br, 1H), 5.89 (s, 1H), 5.86 (s, 1H), 5.70 (dd, J = 8.4, 7.2 Hz, 1H), 4.95 (s, 2H), 4.69 (dd, J = 11.0, 7.2 Hz, 1H), 4.57 (dd, J = 11.0, 8.4 Hz, 1H), 4.29 (dd, J = 9.3, 3.9 Hz, 1H), 3.88 (q, J = 7.1 Hz, 1H), 3.80 (s, 3H), 3.46 (dd, J = 13.7, 3.9 Hz, 1H), 3.21 (dd, J = 13.7, 9.3 Hz, 1H), 2.21 (s, 3H), 2.09 (s, 3H), 2.05 (s, 3H), 1.45 (d, J = 7.1 Hz, 3H); ¹³C NMR (100 MHz, CDCI₃) δ 170.7, 168.7, 166.5, 151.8, 15.0, 151.0, 147.0, 139.0, 136.7, 134.5, 133.2, 128.6, 128.4, 128.2, 128.1, 111.8, 109.1, 106.3, 100.9, 97.3, 74.6, 62.7, 60.4, 57.0, 55.0, 44.9, 21.2, 20.8, 15.5, 8.7; major isomer; IR (neat film) 3374, 1751, 1683, 1651, 1430, 1314, 1265, 1233, 1094, 1040, 1006 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ (d, J = 8.3 Hz, 2H), 7.36-7.43 (m, 3H), 6.86 (s, 1H), 6.40 (s, 1H), 5.93 (2, 1H), 5.92 (s, 1H), 5.62 (dd, J = 8.9, 5.8 Hz, 1H), 5.50 (s, 1H), 5.15 (br, 1H), 5.03 (d, J = 6.8 Hz, 1H), 5.021 (d, J = 6.8 Hz, 1H), 4.76 (dd, J = 11.7, 8.9 Hz, 1H), 4.60 (dd, 11.7, 5.8 Hz, 1H), 4.34 (dd, J = 10.7, 3.9 Hz, 1H), 4.18 (q, J = 7.1 Hz, 1H), 3.84 (s, 3H), 3.81 (dd, J = 14.2, 3.9 Hz, 1H), 2.84 (dd, J = 14.2, 10.7 Hz, 1H), 2.25 (s, 3H), 2.13 (s, 3H), 2.07 (s, 3H), 1.15 (d, J = 7.1 Hz, 1H); ¹³C MHz, CDCl₃) δ 170.7, 170.3, 166.9, 152.2, 151.0, 150.8, 146.8, 138.9, 136.6, 134.1, 133.4, 128.6, 128.4, 128.3, 128.2, 112.5, 108.9, 106.5, 101.0, 96.2, 74.6, 62.0, 60.4, 54.9, 53.3, 52.5, 41.5, 20.8, 18.0, 15.6, 8.7; Synthesis of Compound 3-4

To the CH₂Cl₂ (100 mol) solution of compound 3-3 (19.3 g, 26.4 mmol) and trimethylamine (11.8 ml, 84.6 mmol), MsCl (2.60 ml, 33.8 mmol) was added at 0° C., then stirred for 1 hour. EtOAc (400 ml) was added to the reaction solution and washed by 1N HCl, saturated NaHCO₃ aqueous solution and brine, then dried by MgSO₄. After concentrated by vacuum, the residue was purified by silica gel chromatography (in 70% EtOAc m-hexane). Thus, the mecyl body (19.4 g, 24.0 mmol, 91%) was obtained as a yellow solid. To the CH₃CN (15 ml) solution of mecyl body (3.00 g, 3.71 mmol) and (Boc)₂O (1.36 g, 6.22 mmol) was added and stirred for 6.5 hours. EtOAc was added to the reaction solution and washed with 0.5N HCl, saturated NaHCO₃ aqueous solution and brine. The organic layer was dried by MgSO₄, concentrated by vacuum and the residue was purified by silica gel chromatography (in 50% EtOAc n-hexane). Thus the compound 3-4 (3.27 g, 3.60 mmol, 97%) was obtained as a yellow solid. The physical property of the compound 3-4 is shown in Table 19.

TABLE 19 Compound 3-4 major isomer; IR (neat film) 1775, 1733, 1670, 1455, 1429, 1368, 1308, 1285, 1244, 1172, 1148, 1066, 970, 937 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.58 (d, J = 6.8 Hz, 2H), 7.33-7.41 (m, 3H), 6.87 (s, 1H), 6.82 (s, 1H), 5.97 (s, 1H), 5.96 (s, 1H), 5.56, (dd, J = 8.0, 8.0 Hz, 1H), 5.14 (dd, J = 8.0, 4.8 Hz, 1H), 4.95 (d, J = 10.0 Hz, 1H), 4.91 (d, J = 10.0 Hz, 1H), 4.63 (dd, J = 10.8, 8.0 Hz, 1H), 4.56 (dd, J = 10.8, 8.0 Hz, 1H), 3.98 (q, J = 8.0, 1H), 3.78 (s, 3H), 3.53 (dd, J = 14.8, 4.8 Hz, 1H), 3.23 (dd, J = 14.8, 8.0 Hz, 1H), 3.16 (s, 3H), 2.20 (s, 3H), 2.19 (s, 3H), 2.03 (s, 3H), 1.45 (d, J = 8.0 Hz, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 170.5, 167.8, 166.0, 151.8, 150.9, 149.5, 147.3, 144.1, 142.5, 136.8, 134.9, 132.9, 128.7, 128.4, 128.4, 128.2, 115.3, 115.1, 113.1, 102.1, 97.5, 84.4, 74.6, 62.0, 60.4, 59.5, 56.5, 56.5, 53.5, 44.6, 38.0, 27.8, 20.8, 20.8, 15.5, 9.9 Synthesis of Compound 3-5

To the EtOH (100 ml) and CH₂Cl₂ (10 ml) mixed solution of the compound 3-4 (4.11 g, 4.52 mmol), H₂SO₄ (3.0 ml, 9.0 mmol in 3.0M EtOH solution) and NaBH₄ (867 mg, 22.9 mmol) were added at 0° C. After acetone (10 ml) was added, neutralized by saturated NaHCO₃ aqueous solution, added EtOAc and filtrated by Cellite. Then concentrated by vacuum, EtOH was added to the residue and washed by saturated NaHCO₃ aqueous solution. The organic layer was dried by MgSO₄, concentrated by vacuum and aminal (4.19 g) was obtained. The obtained aminal is dissolved in toluene (40 ml), CSA (1.07 g, 4.61 mmol) and quinoline (0.82 ml, 7.0 mmol) are added and heat refluxed for 3 hours. EtOAc is added to the reaction solution and washed by 1N HCl aqueous solution, saturated NaHCO_(a) aqueous solution and brine aqueous solution. The organic layer is dried by MgSO₄, concentrated by vacuum and the residue was purified by silica gel chromatography (in 50% EtOAc n-hexane). Thus the compound 3-5 (3.54 g, 3.97 mmol, 88%) was obtained as a yellow solid. The physical property of the compound 3-5 is shown in Table 20.

TABLE 20 Compound 3-5 [α]_(D) ²⁷+2.9° (c = 2.97, CHCl₃); IR (neat film) 1742, 1692, 1463, 1418, 1362, 1336, 1240, 1172, 1065, 1005, 962, 890, 805 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.60 (d, J = 6.8 Hz, 2H), 7.36-7.44 (m, 3H), 6.87 (br, 1H), 6.69 (s, 1H), 6.21 (s, 1H), 6.01 (s, 1H), 5.96 (s, 1H), 4.97 (s, 2H), 4.93 (br, 1H), 4.85 (br, 2H), 3.80 (s, 3H), 3.19 (s, 3H), 2.91 (br, 2H), 2.22 (s, 3H), 2.20 (s, 3H), 2.04 (s, 3H), 1.32 (s, 9H); ¹³C NMR (100 MHz, CDCl₃) δ 170.3, 151.5, 151.3, 151.1, 150.9, 150.1, 150.1, 150.1, 146.7, 143.1, 143.0, 142.2, 142.1, 136.7, 136.6, 135.8, 134.7, 134.7, 132.0, 131.5, 129.2, 129.1, 128.4, 128.2, 127.9, 127.9, 127.9, 127.7, 126.2, 121.3, 120.8, 115.4, 115.2, 114.0, 113.9, 101.7, 97.0, 96.5, 80.8, 80.7, 77.3, 77.2, 77.0, 76.7, 74.2, 62.4, 62.3, 60.1, 60.0, 57.2, 55.7, 39.1, 38.8, 37.4, 37.4, 27.8, 27.5, 20.4, 16.3, 15.2, 9.6; Synthesis of Compound 3-6

Pd₂(dba)₃ (325 mg, 0.36 mmol, 5 mol %) was added to CH₃CN (50 ml) solution of the compound 3-5 (6.27 g, 7.02 mmol), P(o-tol)₃ (428 mg, 1.41 mmol, 0.2 equivalent) and triethylamine (4.0 ml, 29 mmol, 4.1 equivalent) and refluxed by heating for 2 hours. After EtOAc was added to the reaction solution and concentrated, EtOAc is added to the residue and washed by 10% citric acid, saturated NaHCO₃ aqueous solution and brine. The organic layer was dried by MgSO₄, concentrated by vacuum and the residue was purified by silica gel chromatography (in 50% EtOAc n-hexane). Thus the compound 3-6 (4.44 g, 5.81 mmol, 83%) was obtained as a yellow solid. The physical property of the compound 3-6 is shown in Table 21.

TABLE 21 Compound 3-6 [α]_(D) ²⁷+38.4° (c = 1.85, CHCl₃); IR (neat film) 1743, 1699, 1636, 1424, 1367, 1309, 1233, 1173, 1113, 1065, 861, 808 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.26-7.70 (m, 5H), 6.60-6.75 (br, 1H), 6.30-6.50 (br, 1H), 5.65-6.20 (br, 3H), 4.20-5.30 (br, 8H), 3.80 (s, 3H), 3.09 (s, 3H), 2.90-3.30 (br, 2H), 2.24 (s, 3H), 2.15 (s, 3H), 1.68 (s, 3H), 1.46 (s, 9H); ¹³C NMR (100 MHz, CDCl₃) δ 170.4, 149.7, 148.8, 147.0, 142.9, 142.6, 137.6, 132.3, 128.5, 127.8, 125.7, 115.2, 115.2, 114.0, 113.2, 113.1, 113.0, 113.0, 112.9, 101.8, 96.3, 95.4, 81.1, 74.1, 73.3, 60.3, 60.2, 59.9, 54.0, 54.0, 52.6, 50.5, 37.5, 31.9, 28.3, 20.1, 15.7, 9.9

Example 4

Processes and all products in each process in synthesis of the compound 4-8 contained in general formula 2 are shown in following synthesis process D.

Detail of Synthesis of D Synthesis of Compound 4-1

2N NaOH aqueous solution (0.5 ml, 1 mmol) was added to MeOH solution (1.5 ml) of the compound 3-6 (120 mg, 0.157 mmol) was added and refluxed by heating for 2.5 hours. Et₂O and water were added to the reaction solution and acidificated by 1N HCl aqueous solution, then extracted by EtOAc. The organic layer was washed by saturated NaHCO₃ aqueous solution and brine and concentrated by vacuum. To the residue, pyridine (0.26 ml, 3.2 mmol) acetic acid anhydride (0.15 ml, 1.6 mmol) and DMPA (1 mg, 0.008 mmol) were added at room temperature. After concentrated by vacuum, the residue was purified by silica gel chromatography (in 30% EtOAc n-hexane). Thus the compound 4-1 (106 mg, 0.145 mmol, 93%) was obtained as a white solid. The physical property of the compound 4-1 is shown in Table 22.

TABLE 22 Compound 4-1 [α]_(D) ²⁶+46.6° (c = 1.27, CHCl₃); IR (neat film) 1766, 1746, 1699, 1634, 1484, 1427, 1368, 1307, 1208, 1183, 1109, 1081, 937, 913, 862; ¹H NMR (40 MHz, CDCl₃) δ 7.26, −7.42 (m, 5H), 6.64 (br, 1H), 6.13 (br, 1H), 5.70-5.95 (br, 3H), 4.15-5.30 (br, 8H), 3.73 (s, 3H), 2.90-3.20 (br, 2H), 2.19 (s, 3H), 2.17 (s, 3H), 1.89 (s, 3H), 1.51 (s, 3H), 1.39 (s, 9H); ¹³C NMR (100 MHz, CDCl₃) δ 170.4, 169.2, 169.1, 149.8, 149.7, 149.7, 148.8, 146.8, 146.7, 144.3, 141.8, 140.4, 137.6, 137.6, 132.1, 132.1, 128.6, 128.5, 128.0, 128.0, 128.0, 127.9, 127.8, 127.7, 127.7, 127.7, 127.6, 127.5, 127.5, 127.5, 127.5, 125.7, 125.7, 125.7, 125.7, 115.3, 115.2, 115.2, 115.2, 115.2, 112.6, 112.2, 112.2, 112.2, 112.2, 101.6, 101.5, 81.0, 81.0, 81.0, 74.1, 74.1, 74.1, 73.6, 60.2, 59.6, 54.0, 52.8, 52.7, 52.7, 52.5, 52.5, 50.8, 50.8, 50.7, 50.7, 50.7, 32.0, 28.3, 20.6, 20.6, 20.0, 15.7, 9.3; Synthesis of Compound 4-2

To the CH₂Cl₂ (12 ml) solution of the compound 4-1 (2.56 g, 3.51 mmol), TFA (3.0 ml, 39 mmol) was added at room temperature and stirred for 4 hours. The reaction solution was poured into saturated NaHCO₃ aqueous solution and extracted by CH₂Cl₂. After organic layer was concentrated by vacuum, the residue is dissolved in CH₂Cl₂ (12 ml) and saturated NaHCO₃ aqueous solution (20 ml) was added. To the reaction solution, TrocCl (0.47 ml, 3.5 mmol) was added and stirred for 10 minutes. The organic layer is dried by MgSO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 40% EtOAc n-hexane). Thus the compound 4-2 (2.08 g, 2.59 mmol, 1.74%) is obtained as a white powder. The physical property of the compound 4-2 is shown in Table 23.

TABLE 23 Compound 4-2 [α]_(D) ²⁶+39.5 39.5 (c = 1.07, CHCl₃); IR (neat film) 1763, 1724, 1684, 1636, 1486, 1429, 1368, 1353, 1298, 1222, 1209, 1184, 1124, 1078, 1031, 913, 863; ¹H NMR (400 MHz, CDCl₃) δ 7.31-7.50 (m 5H), 6.72 & 6.74 (s, 1H), 6.22 & 6.20 (s, 1H), 6.00 & 5.96 (s, 1H), 5.87 & 5.77 (s, 2H), 4.50-5.25 (m, 9H), 4.37 & 4.29 (s, 1H), 3.79 (s, 3H), 3.10-3.30 (m 2H), 2.25 (s, 3H), 2.24 (s, 3H), 1.95 (s, 3H), 1.55 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 170.3, 169.2, 149.8, 144.3, 141.8, 137.4, 132.5, 128.5, 128.5, 127.9, 127.8, 127.6, 125.7, 124.8, 115.0, 112.5, 112.2, 101.5, 95.1, 75.0, 74.0, 73.8, 60.2, 53.9, 53.3, 52.5, 32.2, 31.8, 20.6, 19.9, 15.7, 9.2; Synthesis of Compound 4-3

To the MeOH (15.0 ml) solution of the compound 4-2 (681 mg, 0.847 mmol) dimethyloxilan (0.1M acetone solution, 15 ml, 1.5 mmol) was added at 0° C. and stirred for 2 hours. To the reaction solution, Na₂SO₄ (10 g) was added and stirred for 10 minutes, then CSA (7.2 mg, 0.03 mmol) was added and the temperature is elevated to room temperature. To the reaction solution, pyridine (25 μl, 0.31 mmol) was added so as to neutralize, then filtrated and concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane) and the methoxy compound was obtained as a yellow powder.

THF solution (0.80 ml) of methoxy compound was added into TFA solution (4.0 ml) of NaBH₃CN (160 mg, 2.54 mmol) at 0° C. and stirred for 40 minutes. CHCl₃ was added to the reaction solution and neutralized by saturated NaHCO₃ aqueous solution. The residue was passed through a column of basic alumina by EtOAc, then concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane). Thus the compound 4-3 (150 mg, 0.182 mmol, 7.4%) was obtained as a white powder. The physical property of the compound 4-3 is shown in Table 24.

TABLE 24 Compound 4-3 [α]_(D) ²²+33.2 (c = 1.23, CHCl₃); IR (neat film) 3510, 1764, 1722, 1664, 1484, 1428, 1369, 1342, 1304, 1227, 1185, 1126, 1062, 938, 911 cm⁻¹; IR NMR (400 MHz, CDCI3) δ 7.54 (d, J = 6.8 Hz, 2H), 7.38-7.48 (m, 3H), 6.83 & 6.80 (s, 1H), 6.36 & 6.33 (s, 1H), 5.78-5.87 (m, 3H), 5.40 (br, 1H), 5.26-5.30 (m, 1H), 5.11-5.16 (m 1H), 4.70-4.93 (m, 3H), 4.52 (br, 1H), 4.44 (m, 1H), 3.91 & 3.87 (s, 3H), 3.55-3.65 (br, 2H), 3.00-3.30 (m, 3H), 2.29 & 2.28 (s, 3H), 2.22 (s, 3H), 1.95 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 170.4, 170.3, 170.2, 169.8, 169.1, 152.0, 151.6, 149.4, 149.0, 148.5, 146.5, 146.4, 144.3, 144.2, 142.0, 142.0, 135.2, 135.2, 133.4, 133.2, 129.4, 129.2, 129.2, 129.1, 129.0, 129.0, 128.9, 127.3, 127.2, 122.3, 121.8, 113.7, 113.5, 113.1, 113.0, 101.7, 101.6, 95.2, 95.1, 77.2, 76.4, 75.2, 75.1, 62.7, 62.6, 6.5, 6.5, 59.5, 53.9, 53.2, 47.5, 46.9, 31.9, 31.6, 2.7, 2.6, 2.6, 15.7, 9.3; Synthesis of Compound 4-4

To the DMF solution (0.10 ml) of the compound 4-3 (101 mg, 0.123 mmol) and imidazole (21.3 mg, 0.313 mmol), TBSCl (28.0 mg, 0.186 mmol) was added at room temperature and stirred for 2 hours. The reaction solution was purified by silica gel chromatography (in 40% EtOAc n-hexane) and silanylether (106 mg, 0.127 mmol, 92%) was obtained as an oil. Silanylether (524 mg, 0.560 mmol) was dissolved in G/GHNO₃ solution (8.0 ml) and stirred for 2.5 hours at 40° C. EtOAc is added to the reaction solution and washed by 1N HCl aqueous solution, saturated NaHCO₃ aqueous solution and brine. The organic layer was dried by Na₂SO₄ and concentrated by vacuum. The residue is purified by silica gel chromatography (in 50% EtOAc n-hexane). Thus the compound 4.4 (405 mg, 0.475 mmol, 85%) is obtained as a yellow powder. The physical property of the compound 4-4 is shown in Table 25.

TABLE 25 Compound 4-4 [α]_(D) ²³−33.7° (c = 1.48, CHCl₃); IR (neat film) 3309, 1723, 1640, 1423, 1345, 1304, 1257, 1133, 1127, 1095, 838 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.35-7.54 (m 5H), 6.87 & 6.83 (s, 1H), 6.30 (br, 1H), 5.35-5.73 (m 5H), 5.17-5.28 (m, 1H), 5.06-5.16 (m, 1H), 4.98 & 4.90 (d, J = 12.0 Hz, 1H), 4.60-4.86 (m, 3H), 4.27-4.40 (m, 3H), 4.08 (br, 1H), 3.80 & 3.74 (s, 3H), 3.15-3.35 (m, 3H), 2.28 (s, 3H), 1.94 & 1.91 (s, 3H), 0.69 & 0.68 (s, 9H), −0.27 & −0.30 (s, 3H), −0.32 & −0.35 (s, 3H); ¹³C NMR (100 MHz, CDCI₃) δ 151.9, 151.3, 150.1, 149.4, 148.7, 146.0, 136.6, 136.4, 133.2, 132.8, 129.2, 129.1, 128.7, 128.7, 128.6, 128.5, 128.4, 128.4, 126.5, 126.3, 123.2, 116.1, 106.3, 106.2, 105.0, 100.2, 95.0, 75.5, 75.3, 75.1, 68.3, 67.3, 63.1, 62.9, 62.0, 60.2, 58.7, 58.7, 53.6, 53.0, 48.8, 47.9, 32.2, 25.5, 17.8, 17.8, 15.6, 15.6, 8.4, 8.4, −5.9, −6.0, −6.1, −6.2 Synthesis of Compound 4-5

To the CH₃CN (6.0 ml) solution of the compound 4-4 (404 mg, 0.474 mmol) and K₂CO₃ (196 mg, 1.42 mmol) BnBr (73.0 μl, 0.615 mmol) was added and refluxed by heat for 1 hour. CHCl₃ was added to the reaction solution and filtrated by Celite, then concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane). Thus the compound 4-5 (409 mg, 0.434 mmol, 91%) was obtained as a yellow powder. The physical property of the compound 4-5 is shown in Table 26.

TABLE 26 Compound 4-5 [α]_(D) ²³−37.4° (c = 2.11, CHCl₃); IR (neat film) 3749, 1717, 1419, 1340, 1253, 1111, 838 cm−1; 1H NMR (400 MHz, CDCl₃) δ 7.30-7.60 (m, 10H), 6.77 & 6.73 (s, 1H), 5.83 (s, 1H), 5.77 (br, 2H), 5.69 (s, 1H), 5.51 (br, 1H), 5.22 & 5.21 (d, J = 10.0 Hz, 1H), 5.14 (br, 1H), 5.00 & 4.88 (d, J = 11.6 Hz, 1H), 4.74 (d, J = 11.6 Hz, 1H), 4.68 (d, J = 10.0 Hz, 1H), 4.59 (d, J = 10.8 Hz, 1H), 4.50 & 4.46 (d, J = 11.6 Hz, 1H), 4.37 & 4.25, (br, 1H), 4.30 & 4.29 (d, J = 10.8 Hz, 1H), 4.05 & 3.95 (br, 2H), 3.80 & 3.75 (s, 3H), 3.13-3.37 (m, 3H), 1.99 & 1.96 (s, 9H), −0.27 & −0.32 (s, 3H), −0.33 & −0.36 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 170.2, 152.1, 152.1, 150.0, 148.8, 146.2, 137.2, 137.1, 136.5, 133.1, 129.2, 128.7, 128.6, 128.6, 128.5, 128.5, 128.0, 127.9, 127.8, 126.4, 126.3, 123.3, 115.8, 108.1, 102.6, 100.6, 75.5, 75.3, 75.2, 70.8, 67.5, 66.7, 63.5, 62.3, 60.3, 60.3, 59.8, 53.4, 52.7, 47.9, 47.2, 32.0, 31.5, 25.5, 22.6, 17.8, 15.5, 14.1, 8.7, −6.0, −6.3 Synthesis of Compound 4-6

To the THF solution (2.0 ml) of the compound 4-5 (224 mg, 0.238 mmol), Red-Al (1.3M toluene solution, 0.25 ml, 0.325 mmol) was added at 0° C. 1N HCl aqueous solution was added to the reaction solution and extracted by ETOAc. The organic layer was washed by saturated NaHCO₃ aqueous solution and brine, dried by MgSO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 30% EtOAc n-hexane). Thus the compound 4-6 (181 mg, 0.195 mmol, 82%) was obtained as a white solid. The physical property of the compound 4-6 is shown in Table 26.

TABLE 27 Compound 4-6 [α]_(D) ²² −37.4° (c = 1.19, CHCl₃); IR (neat film) 1717, 1435, 1263, 1118, 1024, 840 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.58 (d, J = 8.0 Hz, 1H), 7.50 (d, J = 6.8 Hz, 1H), 7.26-7.49 (m, 8H), 6.77 & 6.73 (s, 1H), 6.41 & 6.40 (s, 1H) 5.86 (s, 1H), 5.77 (s, 1H), 5.57 & 5.51 (s, 1H), 5.41 (br, 1H), 5.21 (dd, J = 10.4, 10.4 Hz, 1H), 4.93 (dd, J = 7.2, 6.0 Hz, 1H), 4.69-5.02 (m, 5H), 4.20-4.35 (m, 3H), 3.87 & 3.83 (s, 3H), 3.74 (m, 1H), 3.14-3.35 (m, 3H), 2.73 (dd, J = 17.6, 6.0 Hz, 1zh9, 2.21 (s, 3H), 2.09 (s, 3H), 0.71 & 0.69 (s, 9H), −0.21 & −0.26 (s, 3H), −0.27 & 0.31 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 153.1, 153.5, 151.8, 149.5, 149.4, 148.1, 147.6, 146.5, 138.2, 137.4, 137.3, 131.4, 131.2, 130.2, 129.9, 128.6, 128.5, 128.4, 128.3, 128.0, 127.9, 127.7, 127.2, 127.2, 125.5, 125.0, 124.4, 120.7, 120.6, 107.9, 101.9, 101.7, 100.7, 100.6, 95.4, 92.1, 92.1, 75.5, 75.2, 75.0, 74.8, 70.3, 68.9, 68.3, 68.1, 66.7, 60.5, 60.3, 60.2, 60.1, 60.0, 59.9, 48.5, 48.1, 47.5, 46.7, 30.7, 30.5, 25.6, 17.8, 15.7, 15.7, 8.7, −5.9, −5.9, −6.0, −6.0 Synthesis of Compound 4-7

To the CH₂Cl₂ (5.0 ml) solution of the compound 4-6 (2.95 g, 0.318 mmol) and TMSCN (127 μl, 0.952 mmol, 3.0 equivalent), BF₃.OEt₂ (in 1.0M CH₂Cl₂ solution, 480 μl, 0.48 mmol) was added at 0° C. The reaction solution was poured into saturated NaHCO₃ aqueous solution, extracted by CH₂Cl₂, and organic layer was dried by MgSO₄ then concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane) and nitrile compound (221 mg, 0.232 mmol) was obtained as a white solid. To the reaction solution of nitrile compound (221 mg, 0.232 mmol), acetic anhydride (1.0 ml) and pyridine (2.0 ml), DMPA (5.6 mg, 0.05 mmol) was added and stirred for 1 hour at room temperature. After reaction solution is concentrated by vacuum, residue is purified by silica gel chromatography (in 30% EtOAc n-hexane) and the compound 4-7 (213 mg, 0.214 mmol, 92%) was obtained as a white solid. Physical properties of the Compound 4-7 are shown in Table 28.

TABLE 28 Compound 4-7 [α]_(D) ²³+49.9° (c = 1.82, CHCl₃); IR (neat film) 1720, 1430, 1251, 1122, 840 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 7.26-7.65 (m, 10H), 6.52, 6.49 (s, 1H), 6.10 (br, 1H), 5.67 (s, 1H), 5.50 & 5.35 (s, 1H), 5.37 (s, 1H), 4.55-5.30 (m, 8H), 5.50-5.55 (m, 3H), 3.89 & 3.83 (s, 3H), 3.65-3.80 8br, 1H), 3.40-3.55 (br, 2H), 2.85 & 2.80 (dd, J = 17.6, 8.0 Hz, 1H), 2.20-2.30 (br, 6H), 1.90-2.00 (br, 3H), 1.53 & 1.65 (d, J = 17.0 Hz, 1H), 0.77 (br, 9H), −0.04 & 0.11 (s, 3H), −0.08 & −0.14 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 170.2, 170.1, 152.6, 152.2, 151.0, 150.8, 149.0, 148.9, 147.6, 147.0, 146.7, 139.7, 139.7, 137.6, 137.4, 137.2, 131.2, 130.9, 130.6, 128.6, 128.6, 128.5, 128.4, 128.1, 128.0, 127.8, 127.7, 127.1, 125.4, 124.9, 124.9, 124.8, 117.9, 1117.9, 117.8, 115.6, 115.6, 109.4, 109.3, 103.6, 103.5, 100.5, 95.2, 95.1, 75.6, 75.1, 74.8, 70.4, 70.2, 63.3, 63.1, 61.9, 61.2, 60.2, 59.3, 54.2, 54.0, 51.8, 51.6, 50.2, 49.3, 49.1, 48.7, 29.8, 29.7, 25.7, 20.8, 20.8, 18.1, 18.1, 15.5, 8.9, −5.7, −5.8, −6.0, −6.1; Synthesis of Compound 4-8

To the CH₃CN (2.0 ml) solution of the compound 4-7 (200 mg, 0.20 mmol), HF (48 wt % aqueous solution, 1.0 ml, 28 mmol) was added and stirred for 3 hours. The reaction solution is poured into saturated NaHCO₃ aqueous solution and extracted by EtOAc. The organic layer was washed by brine and concentrated by vacuum. The residue was purified by silica gel chromatography (in 40% AcOEt n-hexane) and alcohol compound (180 mg, 0.20 mmol, 100%) was obtained as a white solid. To the CH₂Cl₂ (2.5 ml) solution of Dess-Martin reagent (103 mg, 0.243 mmol) was added at room temperature and stirred for 30 minutes. Reaction was stopped by adding 2-propanol (20 μL), then Et₂O was added, filtrated by Celite and concentrated by vacuum. The residue was dissolved in EtOAc and washed by saturated NaHCO₃ aqueous solution and brine. The organic layer was dried by MgSO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 40% EtOAc n-hexane) and the compound 4-8 (165 mg, 0.188 mmol, 92%) was obtained as a white solid. Dess-Martin reagent is shown by following chemical formula.

Physical properties of the Compound 4-7 are shown in Table 29.

TABLE 29 Compound 4-8 [α]_(D) ²⁴+23.2° (c = 0.90, CHCl₃); IR (neat film) 1732, 1607, 1584, 1488, 1382, 1315, 1238, 1122, 1035, 939, 906, 826 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 9.17 & 9.12 (d, 2.8H), 7.23-7.45 (m, 10H), 6.61 & 6.59 (s, 1H), 5.93 (br, 1H), 5.80 (br, 1H), 5.75 & 5.72 (br, 1H), 5.62 (br, 1H), 5.21 & 5.18 (d, J = 10.8 Hz, 1H), 4.65-5.00 (m, 8H), 4.27-4.52 (M, 3H), 3.78 & 3.71 (s, 3H), 3.68 (br, 1H), 3.13 & 3.08 (dd, J = 17.6, 8.0 Hz, 1H), 2.12 (br, 1H), 2.04-2.11 (br, 6H), 2.01 & 2.01 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 196.9, 196.4, 170.2, 152.4, 152.1, 146.7, 139.8, 137.1, 137.1, 132.0, 130.5, 128.6, 128.5, 128.4, 128.0, 127.9, 127.9, 127.8, 127.2, 127.2, 127.0, 125.0, 124.9, 123.9, 113.5, 113.4, 110.4, 103.9, 100.9, 95.0, 75.3, 74.4, 70.5, 70.4, 68.9, 68.4, 62.3, 60.5, 56.8, 51.8, 51.7, 50.1, 49.1, 47.2, 30.0, 20.9, 15.8, 9.0 Synthesis of Compound 4-8

THF (1.2 ml) solution of the compound 4-8 (51.2 mg, 0.058 mmol) and 10% Pd—C (51.1 mg, 0.024 mmol) was stirred for 18 hours at room temperature under the 1 atmospheric pressure of hydrogen gas. The reaction solution was filtrated by Cellite and concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane) and the compound 4-9 (34.2 mg, 0.049 mmol, 84%) was obtained as a yellow film. Physical properties of the Compound 4-7 are shown in Table 30.

TABLE 30 Compound 4-9 [α]_(D) ²⁴+23.1° (c = 1.37, CHCl₃); IR (neat film) 3749, 1722, 1623, 1587, 1501, 1435, 1380, 1317, 1265, 1232, 1127, 1105, 1056, 1032, 1012, 965 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 6.55 (s, 1H), 5.92 (s, 1H), 5.85 & 5.80 (s, 1H), 5.83 8s, 1H), 4.91 & 4.87 (d, J = 8.0 Hz, 1H), 4.87 & 4.85 8d, J = 11.6 Hz, 1H), 4.69 & 4.67 (d, J = 11.6 Hz, 1H), 4.48 (d, 10.4 Hz, 1H), 4.46 (m, 1H), 4.19 (br, 1H), 4.07 (br, 1H), 3.77 & 3.76 (s, 3H), 3.66 (dd, J = 10.8, 8.0 Hz, 1H), 3.34 & 3.31 (dd, J = 10.4, 2.8 Hz, 1H), 3.25 (dd, J = 17.6, 8.0 Hz, 1H), 2.85 & 2.80 (d, J = 17.6 Hz, 1H), 2.25 & 2.24 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 170.3, 153.1, 152.5, 149.3, 149.2, 145.9, 145.9, 144.0, 143.7, 142.5, 142.3, 135.4, 135.3, 131.6, 131.3, 130.1, 130.1, 123.1, 122.9, 117.0, 116.9, 115.9, 115.8, 110.0, 109.9, 108.0, 101.0, 95.3, 95.0, 75.3, 75.1, 68.9, 68.8, 64.1, 61.6, 61.5, 61.1, 61.0, 58.9, 58.8, 56.3, 49.6, 48.9, 47.1, 46.4, 30.5, 29.6, 20.2, 15.7, 15.7, 8.6

Example 5

Synthesis of compounds contained in general formula 1. Each process from reaction 5-1 to reaction 5-3 and products from each process are shown in synthetic process E.

Details of Synthetic Process E Synthesis of Compound 5-1

To the CH₂Cl₂ (1.2 ml) solution of the compound 4-9 (34.2 mg, 0.049 mmol) and i-Pr₂NEt (0.20 ml, 1.2 mmol), AllylBr (40 μl, 0.47 mmol) was added and heat refluxed for 3 hours. CH₂Cl₂ was added to the reaction solution, washed by 1N HCl aqueous solution, saturated NaHCO₃ aqueous solution and brine. The organic layer was dried by MgSO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane) and allylether (32.3 mg, 0.044 mmol, 89%) was obtained. To the MeOH (0.6 ml) solution of the allylether (32.3 mg, 0.044 mmol), K₂CO₃ (70.8 mg, 0.51 mmol) was added and stirred for 30 minutes at room temperature. EtOAc was added to the reaction solution, and washed by 10% citric acid, saturated NaHCO₃ aqueous solution and brine. The organic layer was washed by MgSO₄ and concentrated by vacuum. The residue was purified by silica gel chromatography (in 50% EtOAc n-hexane) and the compound 5-1 (30.3 mg, 0.044 mmol, 99%) was obtained as a colorless film. Physical properties of the Compound 5-1 are shown in Table 31.

TABLE 31 Compound 5-1 [α]_(D) ²⁶+43.8° (c = 1.11, CHCl₃); IR (neat film) 3298, 1720, 1486, 1434, 1378, 1336, 1315, 1267, 1229, 1125, 1058, 1032, 965, 827 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 9.59 & 9.57 (s, 1H), 6.81 & 6.78 (s, 1H), 6.20 (m, 1H), 5.65-5.95 (m, 4H), 5.40-5.60 (m, 2H), 4.60-5.00 (m, 4H), 4.50 (m, 2H), 4.20-4.40 (m, 2H), 4.00 (m, 1H), 3.84 & 3.82 (s, 3H), 3.60 (m, 1H), 3.20-3.35 (m, 3H), 2.86 (d, J = 17.6 Hz, 1H), 2.24 & 2.23 (s, 3H), 2.06 & 2.04 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 152.8, 152.2, 149.4, 149.3, 148.7, 147.4, 147.0, 145.8, 135.4, 135.3, 133.0, 132.7, 132.0, 130.5, 130.1, 126.5, 126.5, 123.8, 123.0, 121.7, 121.3, 115.7, 115.7, 110.2, 109.5, 109.4, 107.9, 100.9, 100.9, 95.1, 15.0, 77.2, 76.1, 75.6, 75.5, 75.2, 68.9, 68.7, 68.5, 65.5, 65.5, 62.0, 61.4, 60.6, 60.6, 59.3, 59.3, 58.3, 58.2, 49.8, 48.6, 47.4, 47.0, 30.7, 30.7, 30.6, 15.8; Synthesis of Compound 5-2

To the CH₂Cl₂ (1.60 ml) solution of the compound 5-1 (51.0 mg, 0.073 mmol) and S-acetyl-N-alloccystein (42.7 mg, 0.173 mmol), WSCD.HCl (37.2 mg, 0.194 mmol) and DMAP (1.9 mg, 0.008 mmol) were added at room temperature. After stirred for 10 minutes, CH₂Cl₂ was added to the reaction solution, and washed by 1N HCl aqueous solution, saturated NaHCO₃ aqueous solution and brine. The organic layer was concentrated by vacuum, and the residue was purified by silica gel chromatography (in 50% EtOAc n-hexane) and ester (64.0 mg, 0.070 mmol, 94%) was obtained as a yellow film.

To the CH₃CN (0.80 ml) solution of ester (29.5 mg, 0.032 mmol), hydrazine solution (upper layer of 1:3 mixture (by volume) of hydrazine hydride and CH₃CN₃, 35 μl) was added and stirred for 1.5 minutes at room temperature. CHCl₃ was added to the reaction solution, washed by 1N HCl aqueous solution, saturated NaHCO₃ aqueous solution and brine and dried by Na₂SO₄. Solution was evaporated off and the compound 5-2 (27.8 mg, 0.03 mmol, 98%) was obtained as a colorless film. Physical properties of the Compound 5-2 are shown in Table 32.

TABLE 32 Compound 5-2 [α]_(D) ²⁴+22.8° (c = 1.11, CHCl₃); IR (neat film) 3297, 1718, 1507, 1436, 1375, 1338, 1298, 1263, 1125, 1102, 1059, 1032, 1013, 968, 939, 827 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 9.50-9.65 (m, 1H), 7.26-7.40 (m, 5H), 6.72-6.83 (m, 1H), 6.23 (m, 1H), 6.12 & 6.09 (d, J = 4.0 Hz, 1H), 5.95 (s, 1H), 5.88 (m, 1H), 5.81, (s, 1H), 5.79 & 5.69 (s, 1H) 5.20-5.60 (m, 4H), 4.77-5.02 (m, 3H), 4.63-4.72 (m, 1H), 4.27-4.64 (m, 4H), 4.08-4.27 (m, 3H), 3.95-4.68 (m, 1H), 3.87 (s, 3H), 3.89 (s, 3H), 3.15-3.35 (m, 2H), 2.70-3.05 (m, 1H), 2.88 8d, J = 17.6 Hz, 1H), 2.50-2.70 (m, 2H), 2.27 & 2.25 (s, 3H), 2.08 (s, 3H), 0.85-1.45 (m, 2H); ¹³C NMR (100 MHz, CDCl₃) δ 169.8, 169.5, 155.3, 152.8, 152.2, 149.6, 149.5, 148.6, 148.5, 147.5, 147.0, 145.9, 135.3, 132.7, 132.5, 132.4, 132.3, 132.0, 132.0, 131.0, 130.6, 126.7, 126.6, 123.9, 123.2, 121.7, 121.6, 121.1, 118.4, 118.2, 118.1, 115.6, 115.6, 110.0, 109.0, 109.2, 108.4, 108.2, 101.0, 95.2, 95.1, 76.2, 75.6, 75.6, 75.3, 68.9, 68.7, 68.6, 66.2, 66.1, 66.0, 65.1, 61.9, 61.4, 60.8, 60.7, 59.1, 58.8, 56.7, 55.2, 55.1, 54.8, 52.8, 49.7, 48.8, 47.1, 46.9, 46.8, 31.6, 30.5, 30.3, 30.1, 27.2, 26.8, 26.5, 22.6, 15.9, 15.8, 15.8, 14.2, 14.1, 8.6; Synthesis of Compound 5-3

To the trifluoroetanol solution of the compound 5-2 (24.6 mg, 0.028 mmol), TFA (10% 2,2,2-trifluoroetanol, 0.15 ml, 0.19 mmol) was added at room temperature and stirred for 3 hours. Benzene was added to the reaction solution and concentrated by vacuum. The obtained residue was dissolved in acetate anhydride (0.1 ml) and pyridine (0.2 ml), then DMAP (1.5 mg, 0.012 mmol) was added and stirred for 30 minutes. The reaction solution was concentrated by vacuum and the residue was purified in PTLC (30% EtOAc n-hexane). The compound 5-3 (18.0 mg, 0.020 mmol, 71%) was obtained as a colorless film. Physical properties of the Compound 5-3 are shown in Table 33.

TABLE 33 Compound 5-3 [α]_(D) ²³−22.2° (c = 1.06, CHCl₃); IR (neat film) 3402, 1759, 1721, 1510, 1431, 1372, 1332, 1309, 1265, 1236, 1193, 1125, 1101, 1-87, 1060, 1029, 1007, 983, 916, 826 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 6.79 & 6.78 (s, 1H), 6.18 (m, 1H), 6.10 (s, 1H), 6.01 & 5.99 (s, 1H), 5.94 (m, 1H), 5.45-5.68 (m, 2H), 5.22-5.35 (m, 3H), 4.97-5.15 (m, 3H), 4.65-4.90 (m, 3H), 4.42-4.63 (m, 5H), 4.33 (br, 1H), 4.15-4.27 (m, 4H), 3.81 & 3.87 (s, 3H), 3.43 (s, 1H), 3.12-3.29 (m, 2H), 2.30-2.38 (m, 2H), 2.29 & 2.28 (s, 3H), 2.26 & 2.25 (s, 3H), 2.03 (s, 3H); 13C NMR (100 MHz, CDCl₃) δ 170.4, 168.6, 168.5, 155.3, 152.6, 152.2, 149.5, 148.8, 148.7, 146.0, 146.0, 141.0, 140.3, 140.3, 134.6, 134.5, 132.9, 132.7, 132.7, 132.6, 130.1, 129.6, 127.1, 126.5, 125.1, 125.0, 119.5, 119.4, 118.1, 116.2, 116.2, 116.2, 116.0, 115.9, 113.9, 112.7, 112.6, 102.1, 102.1, 95.2, 95.0, 75.3, 75.3, 73.4, 72.7, 65.9, 61.3, 61.3, 60.4, 60.4, 59.4, 59.4, 58.4, 58.2, 58.0, 57.7, 53.8, 49.0, 48.1, 47.9, 47.7, 41.2, 41.1, 32.9, 32.9, 28.1, 27.7, 20.5, 20.4, 15.8, 15.8, 9.6; Reference Example 1

Processes and products at each process regarding the synthesis of ecteinascidin 743 from the compound 5-3 is shown in following synthetic process F.

Detail of Synthesis of F Synthesis of Compound 6-1

To the Et₂O (0.40 ml) solution of the compound 5-3 (17.3 mg, 0.0190 mmol) and zinc powder (96.1 mg, 1.47 mmol), AcOH (0.20 ml) was added at room temperature and stirred for 2.5 hours. Reaction solution was filtrate by Celite and concentrated by vacuum. EtOH was added to the residue and washed by saturated NaHCO₃ and brine. The organic layer was concentrated by vacuum and the residue was purified refined by PTLC (in 50% EtOAc n-hexane), thus amine (12.8 mg, 0.0175 mmol, 92%) was obtained as a colorless film. To amine (5.6 mg, 0.0076 mmol), aqueous solution (30 μl) of formalin and MeOH (0.4 ml) solution of NaBH₃CN (12 mg, 0.19 mmol), AcOH (0.10 ml) was added and stirred at room temperature for 1 hour. After concentrated by vacuum, the reaction solution was diluted by EtOAc and washed by saturated NaHCO₃ and brine. The organic layer was concentrated by vacuum, and the residue was purified by PTLC (in 50% EtOAct n-hexane), then the compound 6-1 (5.5 mg, 0.0074 mmol, 96%) was obtained as a colorless film. Physical properties of the Compound 6-1 are shown in Table 34.

TABLE 34 Compound 6-1 [α]_(D) ²³−25.6° (c = 0.86, CHCl₃); IR (neat film) 3401, 1759, 1724, 1507, 1446, 1372, 1331, 1235, 1194, 1145, 1106, 1088, 1067, 998, 915 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 6.78 (s, 1H), 6.08 (s, 1H), 6.08 (m, 1H), 5.99 (s, 1H9, 5.96 (m, 1H), 5.45 (d, J = 17.6 Hz, 1H), 5.31 (d, J = 17.6 Hz, 1H), 5.25 (d, J = 10.8 Hz, 2H), 5.02 (d, J = 12.0 Hz, 1H), 4.80 (m, 2H), 4.40-4.55 (m, 3H), 4.27-4.40 (m, 2H), 4.24 (s, 1H), 4.19 (m, 1H), 4.16 (m, 2H), 3.79 (s, 3H), 3.35-3.45 (m 2H), 2.85-2.97 (m, 2H), 2.29 (s, 3H), 2.27 (s, 3H), 2.20-2.40 (m, 1H), 2.20 (s, 3H), 2.13 (d, J = 16.4 Hz, 1H), 2.03 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 170.4, 168.6, 155.4, 150.8, 148.8, 145.7, 140.9, 140.3, 134.5, 132.8, 131.7, 129.9, 124.7, 124.6, 120.2, 118.0, 116.6, 113.5, 113.3, 102.0, 72.9, 65.8, 61.3, 60.4, 59.2, 59.1, 55.0, 54.5, 53.8, 41.6, 41.5, 32.8, 23.7, 20.4, 15.7, 9.6 Synthesis of Compound 6-2

To the CH₂Cl₂ (0.70 ml) solution of the compound 6-1 (8.6 mg, 0.012 mmol), Pd(PPh₃)Cl₂ (3.2 mg, 0.0045 mmol) and AcOH (15 μl, 0.26 mmol, 23 equivalent), n-Bu₃SnH (30 μl, 0.11 mmol) was added at room temperature for 20 minutes. The reaction solution was diluted by Et₂O, and after filtrated by Celite, concentrated by vacuum. The residue was refined by silica gel chromatography (in 10% MeOH CH₂Cl₂) and amine (6.4 mg, 0.010 mmol, 89%) was obtained as a white film.

To the mixed solvent of DMF (0.15 ml) and CH₂Cl₂ (0.15 ml) of amine (3.7 mg, 0.0059 mmol), 4-formyl-N-methylpyridine (16.5 mg, 0.057 mmol, 10 equivalent) was added and stirred at room temperature for 15 min. DBU (8.0 μl, 0.053 mmol) was added to the reaction solution and stirred at room temperature for 15 min. The reaction solution was diluted by CH₂Cl₂ (0.30 ml), then saturated citric acid aqueous solution (100 μl) was added and stirred for 40 minutes. Saturated NaHCO₃ aqueous solution and Et₂O were added, then Et₂O layer was concentrated by vacuum. The residue was purified by PTLC (in 70% EtOAc n-hexane), and the compound 6-2 (2.0 mg, 0.0032 mmol, 54%) was obtained as a white film. Physical properties of the Compound 6.2 are shown in Table 35.

TABLE 35 Compound 6-2 [α]_(D) ²²+153° (c = 0.20, CHCl₃); IR (neat film) 3447, 1763, 1723, 1622, 1589, 1500, 456, 373, 1270, 1236, 1194, 1160, 1145, 1108, 1087, 1063 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 6.49 (s, 1H), 6.11 (s, 1H), 6.03 (s, 1H), 5.69 (s, 1H), 5.09 (d, J = 11.6 Hz, 1H), 4.66 (br, 1H), 4.39 (s, 1H), 4.24 (d, J = 4.8 Hz, 1H), 4.22 (d, J = 11.6 Hz,, 1H), 4.16 (d, J = 2.8 Hz, 1H), 3.76 (s, 3H), 3.54 (d, J = 4.8 Hz, 1H), 3.43 (dd, J = 9.6, 2.8 Hz, 1H), 2.90 (dd, J = 18.4, 9.6 Hz, 1H), 2.84 (d, J = 13.6 Hz, 1H), 2.70 (d, J = 18.4 Hz, 1H), 2.57 (d, J = 13.6 Hz, 1H), 2.33 (s, 3H9, 2.24 (s, 3H), 2.14 (s, 3H), 2.04 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 186.7, 168.5, 160.5, 147.1, 146.4, 142.9, 141.6, 140.7, 130.4, 129.8121.7, 121.7, 120.0, 117.9, 117.1, 113.5, 113.3, 102.2, 61.7, 61.4, 60.3, 59.8, 58.9, 54.6, 43.2, 41.6, 36.8, 24.1, 20.4, 15.8, 9.7 Synthesis of Compound 6-3

To the EtOH (0.25 ml) solution of the compound 6-2 (2.0 mg, 0.0026 mmol) and 3-hydroxy-4-methoxyphenylethylamine (12.4 mg, 0.062 mmol), NaOAc (7.4 mg, 0.090 mmol) was added at room temperature and stirred for 5.5 hours. After concentrated by vacuum, the residue was purified by PTLC (5% MeOH in CH₂Cl₂) and the compound 6-3 (2.4 mg, 0.0031 mmol, 96%) was obtained as a white film. Physical properties of the Compound 6-3 are shown in Table 36.

TABLE 36 Compound 6-3 [α]_(D) ²³−57.0° (c = 0.24, CHCl₃); IR (neat film) 3437, 2931, 1743, 1591, 1507, 1456, 1369, 1236, 1193, 1107, 1087, 1053, 1028 cm⁻¹; ¹H NMR (400 MHz, CDCl₃) δ 6.60 (s, 1H), 6.48 (s, 1H), 6.45 (s, 1H), 6.05 (s, 1H), 5.98 (s, 1H), 5.73 (s, 1H), 5.38 (br, 1H), 5.02 (d, J = 11.6 Hz, 1H), 4.57 (br, 1H), 4.33 (s, 1H), 4.28 (d, J = 5.2 Hz, 1H), 4.19 (d, J = 2.8 Hz, 1H), 4.12 (dd, J = 11.6, 2.8 Hz, 1H), 3.79 (s, 3H), 3.63 (s, 3H), 3.51 (d, J = 4.8 Hz, 1H), 3.42 (m, 1H), 3.10 (ddd, J = 11.6, 10.8, 4.0 Hz, 1H), 2.94 (m, 2H), 2.78 (m, 1H), 2.62 (m, q1H), 2.47 (m, 1H), 2.35 (m, 1H), 2.32 (s, 3H), 2.27 (s, 3H), 2.20 (s, 3H), 2.09 (m, 1H), 2.04 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 172.6, 168.1, 147.8, 145.3, 144.5, 144.3, 143.0, 141.3, 140.1, 130.8, 129.3, 129.1, 125.8, 121.2, 120.7, 118.2, 118.1, 114.1, 114.1, 113.4, 109.8, 101.9, 64.6, 61.1, 60.4, 60.0, 59.7, 59.5, 55.2, 54.7, 54.6, 42.2, 41.8, 41.6, 39.6, 28.8, 24.2, 20.5, 15.8, 9.7; Synthesis of Compound 6-4

To the CH₂CN (0.3 ml) and H₂O (0.2 ml) mixed solution of the compound 6-3 (2.4 mg, 0.031 μmmol, 1.0 equivalent), AgNO₃ (10.2 mg, 0.060 mmol) was added and stirred at room temperature for 17 hours. EtOAc was added to the reaction solution, washed by saturated NaHCO₃ aqueous solution and the organic layer was dried by Na₂SO₄. Then concentrated by vacuum, and the compound 6-4 was obtained as a yellow film. Physical properties of the Compound 6-4 are shown in Table 37.

TABLE 37 Compound 6-4 [α]_(D) ²²−58.0° (c = 0.15, CH₂Cl₂); IR (neat film) 3347, 2930, 1763, 1741, 1590, 1509, 1458, 1431, 1369, 1237, 1195, 1122, 1109, 1088, 1053, 1029, 1003, 958, 916 cm⁻¹; ¹H NMR (400 MHz,) δ 6.61 (s, 1H), 6.47 (s, 1H), 6.45 (s, 1H), 6.02 (s, 1H), 5.94 (s, 1H), 5.69 8br, 1H), 5.39 (br, 1H), 5.13 (d, J = 11.2 Hz, 1H), 4.81 (s, 1H), 4.48 (d, J = 3.3 Hz, 1H), 4.48 (br, 1H), 4.16 (d, J = 5.1 Hz, 1H), 4.05 (dd, J = 11.2 Hz, 1H), 3.79 (s, 3H), 3.62 (s, 3H), 3.57 8d, J = 4.9 Hz, 1H), 3.22 (br, 1H), 3.12 (ddd, J = 10.0, 10.0, 4.0 Hz, 1H), 2.82-2.97 (m, 2H), 2.81 (m, 1H), 2.60 (ddd, J = 15.9, 10.0, 4.0 Hz, 1H), 2.48 (ddd, J = 15.9, 4.0, 3.4 Hz, 1H), 2.37 (br, 1H), 2.32 (s, 3H), 2.27 (s, 3H), 2.20 (s, 3H), 2.19 (br, 1H), 2.03 (s, 3H); ¹³C NMR (100 MHz, CDCl₃) δ 172.6, 168.3, 147.7, 145.1, 144.4, 144.2, 142.9, 141.3, 140.5, 131.5, 129.2, 129.1, 121.8, 120.9, 117.9, 115.9, 114.0, 112.5, 109.8, 101.7, 82.1, 64.7, 61.3, 60.4, 57.8, 57.7, 56.0, 55.1, 54.9, 42.2, 42.1, 41.4, 39.7, 28.9, 24.1, 20.5, 15.8, 9.7;

Illustration list of abbreviations MOMO: methoxymethoxy TFA: trifluoroacetic acid TF: trifluoromethansulfonyl Silyl groups TIPS: tri isopropylsilyl group TBS: t-butyldimethyl silyl group TBDPS: t-butyl diphenyl silyl group TES: triethylsilyl group TMS: trimethylsilyl group Dppf: diphenyl phosphiferrocene Ts p-toluenesulfonyl CSA: camphor sulfonic acid Bn: benzyl TMG: N, N, N, N-tetramethylguanidine PMP: paramethoxyphenyl TABF: tetrabutylammonium florid DMAP: dimethylaminopyridine Ms: methansulfonyl TEM: triethylamine Boc: tertiary buthoxycarbonyl Dba: trans,trans-dibenzylidene acetone Troc: trichloroethoxycarbonyl G/GHNO₃: guanidineaqueous solution Red-AI: [(MeOCH₂CH₂)₂ AlH₂] Na Alloc: allyloxycarbonyl WSCDD.HCl: 1-(dimethylaminopropyl)-3-ethylcarbodiimide hydrochloric acid salt

-   DBU: diazabicyclo[5,4,0]undecene-7-en

INDUSTRIAL APPLICABILITY

As mentioned above, by utilizing the intermediates and reaction processes of the present invention, various intermediates and analogues of Et743 can be provided, further excellent effect that these compounds can be effectively produced is provided. 

1. An intermediate compound represented by formula 3, wherein the carbon at a 10^(th) site at a backbone of a 5 membered ring structure of ecteinascidins is bonded with H,

wherein, Y is oxygen or NH, R₁ and R₄ are H or an alkyl group of carbon number 4 or less, R₂ is an alkoxycarbonyl group which can be substituted by halogen, a lower alkyl sulfonyl or an aryl sulfonyl group, X₁ is a hydrogen, a protecting group of an amino group or silyl groups consisting of an acyl group of carbon number 4 or less, t-butyldiphenylsilyl (TBDPS), triisopropylsilyl (TIPS), t-butyldimethylsilyl (TBS), triethylsilyl (TES), and trimethylsilyl (TMS), X₂, X₃ and X₄ are independently selected from the group consisting of H or an alkyl group of carbon number 4 or less, an alkoxyalkyl group, an allyl group, or an alkyl or arylsulfonyl group.
 2. The intermediate compound of claim 1, wherein Y is O, X₁ is selected from silyl groups consisting of an acyl group of carbon number 4 or less, t-butyldiphenylsilyl (TBDPS), triisopropylsilyl (TIPS), t-butyldimethylsilyl (TBS), triethylsilyl (TES), and trimethylsilyl (TMS), X₂ and X₃ are allyl groups, or alkoxy groups of carbon number 4 or less or alkoxyalkyl groups, and R₄ is an alkyl group of carbon number 4 or less.
 3. The intermediate compound of claim 1 produced by the processes displayed by reactions 3-1, 3-2, 3-3, 3-4, 3-5 and 3-6,

wherein, the reaction 3-1 is a connecting reaction of 4 components, the reaction 3-2 is a transforming reaction of C₂₂ t-butyltriphenylsilyl (TBTPS) group to an acetyl group, the reaction 3-3 is a ring forming reaction of C ring formation, the reaction 3-4 is a transforming reaction of C₅ hydroxyl group to a methansulfonyl (Ms) group, the reaction 3-5 is a reducing reaction of C₁₁ amide and a dehydration reaction of C₃₋₄ double bond and the reaction 3-6 is a ring forming reaction of D ring by a Heck reaction, wherein Y is O, X₁ is Ac, X₂ is Ms and R₂ is Boc. 